Canonical Allele Identifier: CA354217800
Gene: ADCY5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.123319705A>G , CM000665.2:g.123319705A>G GRCh38
NC_000003.11:g.123038552A>G , CM000665.1:g.123038552A>G GRCh37
NC_000003.10:g.124521242A>G NCBI36
NG_033882.1:g.133841T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000466617.6:c.902T>C ENSP00000420082.2:p.Leu301Pro
ENST00000470367.2:c.1190T>C ENSP00000514541.1:p.Leu397Pro
ENST00000483566.2:c.902T>C ENSP00000420252.2:p.Leu301Pro
ENST00000699714.1:c.902T>C ENSP00000514539.1:p.Leu301Pro
ENST00000699715.1:c.902T>C ENSP00000514540.1:p.Leu301Pro
ENST00000699716.1:c.902T>C ENSP00000514542.1:p.Leu301Pro
ENST00000699718.1:c.2225T>C ENSP00000514543.1:p.Leu742Pro
ENST00000699719.1:n.484T>C
ENST00000462833.6:c.2225T>C MANE Select ENSP00000419361.1:p.Leu742Pro
ENST00000309879.9:c.1175T>C ENSP00000308685.5:p.Leu392Pro
ENST00000462833.5:c.2225T>C ENSP00000419361.1:p.Leu742Pro
ENST00000466617.5:c.902T>C ENSP00000420082.1:p.Leu301Pro
ENST00000491190.5:c.1124T>C ENSP00000418537.1:p.Leu375Pro
NM_001199642.1:c.1175T>C NP_001186571.1:p.Leu392Pro
NM_183357.2:c.2225T>C NP_899200.1:p.Leu742Pro
XM_005247077.2:c.2225T>C XP_005247134.1:p.Leu742Pro
XM_005247078.1:c.1175T>C XP_005247135.1:p.Leu392Pro
XM_006713483.1:c.1124T>C XP_006713546.1:p.Leu375Pro
XM_006713484.1:c.902T>C XP_006713547.1:p.Leu301Pro
XM_011512358.1:c.2225T>C XP_011510660.1:p.Leu742Pro
XM_011512359.1:c.1226T>C XP_011510661.1:p.Leu409Pro
XM_011512360.1:c.1136T>C XP_011510662.1:p.Leu379Pro
XM_011512361.1:c.902T>C XP_011510663.1:p.Leu301Pro
XM_005247077.4:c.2225T>C XP_005247134.1:p.Leu742Pro
XM_011512359.2:c.1226T>C XP_011510661.1:p.Leu409Pro
XM_011512360.3:c.1136T>C XP_011510662.1:p.Leu379Pro
XM_017005638.1:c.1127T>C XP_016861127.1:p.Leu376Pro
XM_017005639.1:c.1127T>C XP_016861128.1:p.Leu376Pro
NM_001378259.1:c.2225T>C NP_001365188.1:p.Leu742Pro
NM_183357.3:c.2225T>C MANE Select NP_899200.1:p.Leu742Pro