Canonical Allele Identifier: CA360733040
Gene: ALDH7A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.126592665T>C , CM000667.2:g.126592665T>C GRCh38
NC_000005.9:g.125928357T>C , CM000667.1:g.125928357T>C GRCh37
NC_000005.8:g.125956256T>C NCBI36
NG_008600.2:g.7726A>G
NG_008600.3:g.7726A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000409134.8:c.311A>G MANE Select ENSP00000387123.3:p.Asp104Gly
ENST00000412186.2:c.311A>G ENSP00000414536.2:p.Asp104Gly
ENST00000413020.6:c.311A>G ENSP00000487936.1:p.Asp104Gly
ENST00000458249.6:c.*220A>G ENSP00000403929.1:n.*220A>G
ENST00000479989.6:n.494A>G
ENST00000503281.6:c.106+2342A>G
ENST00000509270.2:c.246+686A>G ENSP00000449318.2:n.246+686A>G
ENST00000509459.6:c.65+2342A>G
ENST00000511266.6:n.1033A>G
ENST00000635851.1:c.309A>G
ENST00000635858.1:n.150A>G
ENST00000635933.1:n.340A>G
ENST00000636062.1:n.206A>G
ENST00000636190.1:n.190A>G
ENST00000636225.1:c.*120A>G ENSP00000490797.1:n.*120A>G
ENST00000636743.1:c.192+2342A>G ENSP00000489725.1:n.192+2342A>G
ENST00000636808.1:c.*120A>G ENSP00000490833.1:n.*120A>G
ENST00000636872.1:c.471A>G ENSP00000490919.1:n.471A>G
ENST00000636879.1:c.311A>G ENSP00000490811.1:p.Asp104Gly
ENST00000636886.1:c.192+2342A>G ENSP00000490371.1:n.192+2342A>G
ENST00000637206.1:c.311A>G ENSP00000489895.1:p.Asp104Gly
ENST00000637272.1:c.311A>G ENSP00000489686.1:p.Asp104Gly
ENST00000637782.1:c.311A>G ENSP00000490024.1:p.Asp104Gly
ENST00000637964.1:c.257A>G ENSP00000490291.1:p.Asp86Gly
ENST00000638008.1:c.*120A>G ENSP00000490400.1:n.*120A>G
ENST00000409134.7:c.311A>G ENSP00000387123.3:p.Asp104Gly
ENST00000412186.1:c.*120A>G ENSP00000414536.1:n.*120A>G
ENST00000413020.5:c.311A>G ENSP00000487936.1:p.Asp104Gly
ENST00000447989.6:c.392A>G ENSP00000414132.2:p.Asp131Gly
ENST00000458249.5:c.471A>G ENSP00000403929.1:n.471A>G
ENST00000479989.5:n.494A>G
ENST00000503281.5:c.106+2342A>G
ENST00000509270.1:c.192+2342A>G ENSP00000449318.1:n.192+2342A>G
ENST00000509459.5:c.65+2342A>G
ENST00000510111.6:c.305A>G ENSP00000447388.1:p.Asp102Gly
ENST00000511266.5:n.266A>G
ENST00000553117.5:c.311A>G ENSP00000448593.1:p.Asp104Gly
NM_001182.4:c.311A>G NP_001173.2:p.Asp104Gly
NM_001201377.1:c.227A>G NP_001188306.1:p.Asp76Gly
NM_001202404.1:c.392A>G NP_001189333.1:p.Asp131Gly
XM_011543417.1:c.-95A>G XP_011541719.1:n.-95A>G
XM_011543417.2:c.-95A>G XP_011541719.1:n.-95A>G
NM_001182.5:c.311A>G MANE Select NP_001173.2:p.Asp104Gly
NM_001201377.2:c.227A>G NP_001188306.1:p.Asp76Gly
NM_001202404.2:c.311A>G NP_001189333.2:p.Asp104Gly