Canonical Allele Identifier: CA1580460339

Gene: ALDH7A1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.126592669C= , CM000667.2:g.126592669C=	GRCh38
NC_000005.9:g.125928361C= , CM000667.1:g.125928361C=	GRCh37
NC_000005.8:g.125956260C=	NCBI36
NG_008600.2:g.7722G=
NG_008600.3:g.7722G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000409134.8:c.307G= MANE Select	ENSP00000387123.3:p.Ala103=
ENST00000412186.2:c.307G=	ENSP00000414536.2:p.Ala103=
ENST00000413020.6:c.307G=	ENSP00000487936.1:p.Ala103=
ENST00000458249.6:c.*216G=	ENSP00000403929.1:n.*216G=
ENST00000479989.6:n.490G=
ENST00000503281.6:c.106+2338G=
ENST00000509270.2:c.246+682G=	ENSP00000449318.2:n.246+682G=
ENST00000509459.6:c.65+2338G=
ENST00000511266.6:n.1029G=
ENST00000635851.1:c.305G=
ENST00000635858.1:n.146G=
ENST00000635933.1:n.336G=
ENST00000636062.1:n.202G=
ENST00000636190.1:n.186G=
ENST00000636225.1:c.*116G=	ENSP00000490797.1:n.*116G=
ENST00000636743.1:c.192+2338G=	ENSP00000489725.1:n.192+2338G=
ENST00000636808.1:c.*116G=	ENSP00000490833.1:n.*116G=
ENST00000636872.1:c.467G=	ENSP00000490919.1:n.467G=
ENST00000636879.1:c.307G=	ENSP00000490811.1:p.Ala103=
ENST00000636886.1:c.192+2338G=	ENSP00000490371.1:n.192+2338G=
ENST00000637206.1:c.307G=	ENSP00000489895.1:p.Ala103=
ENST00000637272.1:c.307G=	ENSP00000489686.1:p.Ala103=
ENST00000637782.1:c.307G=	ENSP00000490024.1:p.Ala103=
ENST00000637964.1:c.253G=	ENSP00000490291.1:p.Ala85=
ENST00000638008.1:c.*116G=	ENSP00000490400.1:n.*116G=
ENST00000409134.7:c.307G=	ENSP00000387123.3:p.Ala103=
ENST00000412186.1:c.*116G=	ENSP00000414536.1:n.*116G=
ENST00000413020.5:c.307G=	ENSP00000487936.1:p.Ala103=
ENST00000447989.6:c.388G=	ENSP00000414132.2:p.Ala130=
ENST00000458249.5:c.467G=	ENSP00000403929.1:n.467G=
ENST00000479989.5:n.490G=
ENST00000503281.5:c.106+2338G=
ENST00000509270.1:c.192+2338G=	ENSP00000449318.1:n.192+2338G=
ENST00000509459.5:c.65+2338G=
ENST00000510111.6:c.301G=	ENSP00000447388.1:p.Ala101=
ENST00000511266.5:n.262G=
ENST00000553117.5:c.307G=	ENSP00000448593.1:p.Ala103=
NM_001182.4:c.307G=	NP_001173.2:p.Ala103=
NM_001201377.1:c.223G=	NP_001188306.1:p.Ala75=
NM_001202404.1:c.388G=	NP_001189333.1:p.Ala130=
XM_011543417.1:c.-99G=	XP_011541719.1:n.-99G=
XM_011543417.2:c.-99G=	XP_011541719.1:n.-99G=
NM_001182.5:c.307G= MANE Select	NP_001173.2:p.Ala103=
NM_001201377.2:c.223G=	NP_001188306.1:p.Ala75=
NM_001202404.2:c.307G=	NP_001189333.2:p.Ala103=