Canonical Allele Identifier: CA13416633
Gene: MADD HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10501320

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47272248G>C , CM000673.2:g.47272248G>C GRCh38
NC_000011.9:g.47293799G>C , CM000673.1:g.47293799G>C GRCh37
NC_000011.8:g.47250375G>C NCBI36
NG_029462.1:g.7873G>C

Transcript Alleles

HGVS Amino-acid change
NM_001135943.1:c.-88-1579G>C VV NP_001129415.1:p.=
NM_001135944.1:c.-88-1579G>C VV NP_001129416.1:p.=
NM_003682.3:c.-88-1579G>C VV NP_003673.3:p.=
NM_130470.2:c.-88-1579G>C VV NP_569826.2:p.=
NM_130471.2:c.-88-1579G>C VV NP_569827.2:p.=
NM_130472.2:c.-88-1579G>C VV NP_569828.2:p.=
NM_130473.2:c.-88-1579G>C VV NP_569829.2:p.=
NM_130474.2:c.-88-1579G>C VV NP_569830.2:p.=
NM_130475.2:c.-88-1579G>C VV NP_569831.1:p.=
NM_130476.2:c.-88-1579G>C VV NP_569832.2:p.=
XM_005253188.1:c.-88-1579G>C XP_005253245.1:p.=
XM_005253189.1:c.-88-1579G>C XP_005253246.1:p.=
XM_005253190.1:c.-88-1579G>C XP_005253247.1:p.=
XM_005253191.1:c.-88-1579G>C XP_005253248.1:p.=
XM_005253192.1:c.-88-1579G>C XP_005253249.1:p.=
XM_005253193.1:c.-88-1579G>C XP_005253250.1:p.=
XM_005253194.1:c.-88-1579G>C XP_005253251.1:p.=
XM_005253195.1:c.-88-1579G>C XP_005253252.1:p.=
XM_005253196.1:c.-88-1579G>C XP_005253253.1:p.=
XM_005253197.1:c.-88-1579G>C XP_005253254.1:p.=
XM_005253198.1:c.-88-1579G>C XP_005253255.1:p.=
XM_005253199.1:c.-88-1579G>C XP_005253256.1:p.=
XM_005253200.1:c.-88-1579G>C XP_005253257.1:p.=
XM_005253201.1:c.-88-1579G>C XP_005253258.1:p.=
XM_005253202.1:c.-88-1579G>C XP_005253259.1:p.=
XM_005253203.1:c.-88-1579G>C XP_005253260.1:p.=
XM_005253204.1:c.-88-1579G>C XP_005253261.1:p.=
XM_005253205.1:c.-88-1579G>C XP_005253262.1:p.=
XM_005253206.2:c.-88-1579G>C XP_005253263.1:p.=
XM_006718360.1:c.-88-1579G>C XP_006718423.1:p.=
XM_006718361.1:c.-88-1579G>C XP_006718424.1:p.=
XM_006718362.1:c.-88-1579G>C XP_006718425.1:p.=
XM_006718363.1:c.-88-1579G>C XP_006718426.1:p.=
XM_011520428.1:c.-88-1579G>C XP_011518730.1:p.=
XM_011520429.1:c.-88-1579G>C XP_011518731.1:p.=
XM_011520430.1:c.-88-1579G>C XP_011518732.1:p.=
XM_011520431.1:c.-88-1579G>C XP_011518733.1:p.=
XM_011520432.1:c.-171G>C XP_011518734.1:p.=
XM_011520433.1:c.-88-1579G>C XP_011518735.1:p.=
XM_011520434.1:c.-88-1579G>C XP_011518736.1:p.=
XM_011520435.1:c.-88-1579G>C XP_011518737.1:p.=
XM_011520436.1:c.-88-1579G>C XP_011518738.1:p.=
XM_011520437.1:c.-88-1579G>C XP_011518739.1:p.=
XM_011520438.1:c.-88-1579G>C XP_011518740.1:p.=
XM_011520439.1:c.-88-1579G>C XP_011518741.1:p.=
XM_011520440.1:c.-142-2315G>C XP_011518742.1:p.=
XR_242830.1:n.128-1579G>C
XR_930922.1:n.128-1579G>C
XM_005253189.3:c.-88-1579G>C
XM_005253196.3:c.-88-1579G>C
XM_005253199.3:c.-88-1579G>C
XM_005253200.2:c.-88-1579G>C
XM_005253201.3:c.-88-1579G>C
XM_005253203.3:c.-88-1579G>C
XM_005253204.3:c.-88-1579G>C
XM_005253205.2:c.-88-1579G>C
XM_017018478.2:c.-88-1579G>C XP_016873967.1:p.=
XM_017018479.2:c.-88-1579G>C XP_016873968.1:p.=
XM_017018480.2:c.-88-1579G>C XP_016873969.1:p.=
XM_017018481.1:c.-88-1579G>C XP_016873970.1:p.=
XM_017018482.2:c.-88-1579G>C XP_016873971.1:p.=
XM_017018483.2:c.-88-1579G>C XP_016873972.1:p.=
XM_017018484.2:c.-88-1579G>C XP_016873973.1:p.=
XM_017018485.2:c.-88-1579G>C XP_016873974.1:p.=
XM_017018486.2:c.-88-1579G>C XP_016873975.1:p.=
XM_017018487.2:c.-88-1579G>C XP_016873976.1:p.=
XM_017018488.1:c.-88-1579G>C XP_016873977.1:p.=
XM_017018489.1:c.-88-1579G>C XP_016873978.1:p.=
XM_017018490.1:c.-88-1579G>C XP_016873979.1:p.=
XM_017018491.2:c.-88-1579G>C XP_016873980.1:p.=
XM_017018492.1:c.-88-1579G>C XP_016873981.1:p.=
XM_017018493.1:c.-88-1579G>C XP_016873982.1:p.=
XM_017018498.1:c.-88-1579G>C XP_016873987.1:p.=
XM_017018499.1:c.-88-1579G>C XP_016873988.1:p.=
XM_017018500.1:c.-88-1579G>C XP_016873989.1:p.=
XM_017018505.2:c.-88-1579G>C XP_016873994.1:p.=
XM_017018506.1:c.-88-1579G>C XP_016873995.1:p.=
XM_017018507.1:c.-88-1579G>C XP_016873996.1:p.=
XM_024448745.1:c.-88-1579G>C XP_024304513.1:p.=
XM_024448746.1:c.-88-1579G>C XP_024304514.1:p.=
XM_024448747.1:c.-88-1579G>C XP_024304515.1:p.=
XM_024448748.1:c.-88-1579G>C XP_024304516.1:p.=
XM_024448749.1:c.-88-1579G>C XP_024304517.1:p.=
XM_024448750.1:c.-88-1579G>C XP_024304518.1:p.=
XM_024448751.1:c.-88-1579G>C XP_024304519.1:p.=
XM_024448752.1:c.-88-1579G>C XP_024304520.1:p.=
XM_024448753.1:c.-88-1579G>C XP_024304521.1:p.=
XM_024448754.1:c.-88-1579G>C XP_024304522.1:p.=
XM_024448755.1:c.-88-1579G>C XP_024304523.1:p.=
ENST00000311027.9:c.-88-1579G>C ENSP00000310933.4:p.=
ENST00000342922.8:c.-88-1579G>C ENSP00000343902.4:p.=
ENST00000349238.7:c.-88-1579G>C ENSP00000304505.6:p.=
ENST00000395336.7:c.-88-1579G>C ENSP00000378745.3:p.=
ENST00000395344.7:c.-88-1579G>C ENSP00000378753.3:p.=
ENST00000402192.6:c.-88-1579G>C ENSP00000384287.2:p.=
ENST00000402799.5:c.-88-1579G>C ENSP00000385585.1:p.=
ENST00000406482.5:c.-88-1579G>C ENSP00000384435.1:p.=
ENST00000407859.7:c.-88-1579G>C ENSP00000384204.3:p.=
ENST00000422579.1:c.-171G>C ENSP00000402364.1:p.=
ENST00000428807.5:c.-8+2498G>C ENSP00000398167.1:p.=
ENST00000444117.5:c.-88-1579G>C ENSP00000413116.1:p.=
ENST00000453571.5:c.-88-1579G>C ENSP00000388255.1:p.=
ENST00000526603.5:n.91+2002G>C
ENST00000534808.1:n.75-2315G>C