Canonical Allele Identifier: CA1580460441
Gene: ALDH7A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.126592723C= , CM000667.2:g.126592723C= GRCh38
NC_000005.9:g.125928415C= , CM000667.1:g.125928415C= GRCh37
NC_000005.8:g.125956314C= NCBI36
NG_008600.2:g.7668G=
NG_008600.3:g.7668G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000409134.8:c.253G= MANE Select ENSP00000387123.3:p.Val85=
ENST00000412186.2:c.253G= ENSP00000414536.2:p.Val85=
ENST00000413020.6:c.253G= ENSP00000487936.1:p.Val85=
ENST00000458249.6:c.*162G= ENSP00000403929.1:n.*162G=
ENST00000479989.6:n.436G=
ENST00000503281.6:c.106+2284G=
ENST00000509270.2:c.246+628G= ENSP00000449318.2:n.246+628G=
ENST00000509459.6:c.65+2284G=
ENST00000511266.6:n.975G=
ENST00000635851.1:c.251G=
ENST00000635858.1:n.92G=
ENST00000635933.1:n.282G=
ENST00000636062.1:n.148G=
ENST00000636190.1:n.132G=
ENST00000636225.1:c.*62G= ENSP00000490797.1:n.*62G=
ENST00000636743.1:c.192+2284G= ENSP00000489725.1:n.192+2284G=
ENST00000636808.1:c.*62G= ENSP00000490833.1:n.*62G=
ENST00000636872.1:c.413G= ENSP00000490919.1:n.413G=
ENST00000636879.1:c.253G= ENSP00000490811.1:p.Val85=
ENST00000636886.1:c.192+2284G= ENSP00000490371.1:n.192+2284G=
ENST00000637206.1:c.253G= ENSP00000489895.1:p.Val85=
ENST00000637272.1:c.253G= ENSP00000489686.1:p.Val85=
ENST00000637782.1:c.253G= ENSP00000490024.1:p.Val85=
ENST00000637964.1:c.199G= ENSP00000490291.1:p.Val67=
ENST00000638008.1:c.*62G= ENSP00000490400.1:n.*62G=
ENST00000409134.7:c.253G= ENSP00000387123.3:p.Val85=
ENST00000412186.1:c.*62G= ENSP00000414536.1:n.*62G=
ENST00000413020.5:c.253G= ENSP00000487936.1:p.Val85=
ENST00000447989.6:c.334G= ENSP00000414132.2:p.Val112=
ENST00000458249.5:c.413G= ENSP00000403929.1:n.413G=
ENST00000479989.5:n.436G=
ENST00000503281.5:c.106+2284G=
ENST00000509270.1:c.192+2284G= ENSP00000449318.1:n.192+2284G=
ENST00000509459.5:c.65+2284G=
ENST00000510111.6:c.247G= ENSP00000447388.1:p.Val83=
ENST00000511266.5:n.208G=
ENST00000553117.5:c.253G= ENSP00000448593.1:p.Val85=
NM_001182.4:c.253G= NP_001173.2:p.Val85=
NM_001201377.1:c.169G= NP_001188306.1:p.Val57=
NM_001202404.1:c.334G= NP_001189333.1:p.Val112=
XM_011543417.1:c.-153G= XP_011541719.1:n.-153G=
XM_011543417.2:c.-153G= XP_011541719.1:n.-153G=
NM_001182.5:c.253G= MANE Select NP_001173.2:p.Val85=
NM_001201377.2:c.169G= NP_001188306.1:p.Val57=
NM_001202404.2:c.253G= NP_001189333.2:p.Val85=