Canonical Allele Identifier: CA1580455155
Gene: ALDH7A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.126577083G= , CM000667.2:g.126577083G= GRCh38
NC_000005.9:g.125912775G= , CM000667.1:g.125912775G= GRCh37
NC_000005.8:g.125940674G= NCBI36
NG_008600.2:g.23308C=
NG_008600.3:g.23308C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000409134.8:c.646C= MANE Select ENSP00000387123.3:p.Leu216=
ENST00000412186.2:c.522C= ENSP00000414536.2:n.522C=
ENST00000413020.6:c.646C= ENSP00000487936.1:p.Leu216=
ENST00000458249.6:c.*555C= ENSP00000403929.1:n.*555C=
ENST00000503281.6:c.235C=
ENST00000509270.2:c.580C=
ENST00000509459.6:c.194C=
ENST00000511266.6:n.1368C=
ENST00000635851.1:c.644C=
ENST00000636062.1:n.541C=
ENST00000636225.1:c.*455C= ENSP00000490797.1:n.*455C=
ENST00000636286.1:n.364C=
ENST00000636743.1:c.526C= ENSP00000489725.1:p.Leu176=
ENST00000636808.1:c.*455C= ENSP00000490833.1:n.*455C=
ENST00000636872.1:c.806C= ENSP00000490919.1:n.806C=
ENST00000636879.1:c.691C= ENSP00000490811.1:p.Leu231=
ENST00000636886.1:c.445C= ENSP00000490371.1:p.Leu149=
ENST00000637206.1:c.646C= ENSP00000489895.1:p.Leu216=
ENST00000637272.1:c.646C= ENSP00000489686.1:p.Leu216=
ENST00000637292.1:c.299C=
ENST00000637782.1:c.646C= ENSP00000490024.1:p.Leu216=
ENST00000637964.1:c.592C= ENSP00000490291.1:p.Leu198=
ENST00000638008.1:c.*588C= ENSP00000490400.1:n.*588C=
ENST00000409134.7:c.646C= ENSP00000387123.3:p.Leu216=
ENST00000413020.5:c.646C= ENSP00000487936.1:p.Leu216=
ENST00000433026.5:n.173C=
ENST00000447989.6:c.727C= ENSP00000414132.2:p.Leu243=
ENST00000458249.5:c.806C= ENSP00000403929.1:n.806C=
ENST00000503281.5:c.235C=
ENST00000509459.5:c.194C=
ENST00000510111.6:c.559C= ENSP00000447388.1:p.Leu187=
ENST00000511266.5:n.477C=
ENST00000553117.5:c.646C= ENSP00000448593.1:p.Leu216=
NM_001182.4:c.646C= NP_001173.2:p.Leu216=
NM_001201377.1:c.562C= NP_001188306.1:p.Leu188=
NM_001202404.1:c.727C= NP_001189333.1:p.Leu243=
XM_011543417.1:c.241C= XP_011541719.1:p.Leu81=
XM_011543417.2:c.241C= XP_011541719.1:p.Leu81=
NM_001182.5:c.646C= MANE Select NP_001173.2:p.Leu216=
NM_001201377.2:c.562C= NP_001188306.1:p.Leu188=
NM_001202404.2:c.646C= NP_001189333.2:p.Leu216=