Canonical Allele Identifier: CA128027
Gene: ADD1 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 18274
dbSNP Id: rs4961

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.2904980G>T , CM000666.2:g.2904980G>T GRCh38
NC_000004.11:g.2906707G>T , CM000666.1:g.2906707G>T GRCh37
NC_000004.10:g.2876505G>T NCBI36
NG_012037.1:g.66124G>T

Transcript Alleles

HGVS Amino-acid change
NM_001119.4:c.1378G>T VV NP_001110.2:p.Gly460Trp
NM_001286645.1:c.1378G>T VV NP_001273574.1:p.Gly460Trp
NM_014189.3:c.1378G>T VV NP_054908.2:p.Gly460Trp
NM_014190.3:c.1378G>T VV NP_054909.2:p.Gly460Trp
NM_176801.2:c.1378G>T VV NP_789771.1:p.Gly460Trp
XM_005247933.1:c.1378G>T XP_005247990.1:p.Gly460Trp
XM_005247934.1:c.1378G>T XP_005247991.1:p.Gly460Trp
XM_005247935.1:c.1378G>T XP_005247992.1:p.Gly460Trp
XM_005247936.1:c.1378G>T XP_005247993.1:p.Gly460Trp
XM_005247937.1:c.1378G>T XP_005247994.1:p.Gly460Trp
NM_001354754.1:c.1378G>T VV NP_001341683.1:p.Gly460Trp
NM_001354755.1:c.1378G>T VV NP_001341684.1:p.Gly460Trp
NM_001354756.1:c.1378G>T VV NP_001341685.1:p.Gly460Trp
NM_001354757.1:c.1378G>T VV NP_001341686.1:p.Gly460Trp
NM_001354758.1:c.1378G>T VV NP_001341687.1:p.Gly460Trp
NM_001354759.1:c.1378G>T VV NP_001341688.1:p.Gly460Trp
NM_001354761.1:c.1378G>T VV NP_001341690.1:p.Gly460Trp
NM_001354762.1:c.1378G>T VV NP_001341691.1:p.Gly460Trp
XM_005247934.2:c.1378G>T
XM_017007703.1:c.1378G>T XP_016863192.1:p.Gly460Trp
XM_017007704.1:c.1378G>T XP_016863193.1:p.Gly460Trp
XM_017007705.1:c.1378G>T XP_016863194.1:p.Gly460Trp
XM_017007706.2:c.1378G>T XP_016863195.1:p.Gly460Trp
XM_017007709.2:c.1378G>T XP_016863198.1:p.Gly460Trp
XM_024453887.1:c.1378G>T XP_024309655.1:p.Gly460Trp
XR_002959706.1:n.1444G>T
XR_002959707.1:n.1655G>T
ENST00000264758.11:c.1378G>T ENSP00000264758.6:p.Gly460Trp
ENST00000355842.7:c.1378G>T ENSP00000348100.3:p.Gly460Trp
ENST00000398123.6:c.1378G>T ENSP00000381191.2:p.Gly460Trp
ENST00000398125.5:c.1378G>T ENSP00000381193.1:p.Gly460Trp
ENST00000398129.5:c.1378G>T ENSP00000381197.1:p.Gly460Trp
ENST00000446856.5:c.*33G>T ENSP00000399828.2:p.=
ENST00000503169.5:n.1653G>T
ENST00000503455.6:c.1378G>T ENSP00000423024.2:p.Gly460Trp
ENST00000513328.6:c.1378G>T ENSP00000421907.2:p.Gly460Trp
ENST00000514940.5:n.495G>T
ENST00000536078.1:n.317G>T