Canonical Allele Identifier: CA1580440338

Gene: ALDH7A1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.126544843G= , CM000667.2:g.126544843G=	GRCh38
NC_000005.9:g.125880535G= , CM000667.1:g.125880535G=	GRCh37
NC_000005.8:g.125908434G=	NCBI36
NG_008600.2:g.55548C=
NG_008600.3:g.55548C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409134.8:c.*122C= MANE Select	ENSP00000387123.3:n.*122C=
ENST00000458249.6:c.*1651C=	ENSP00000403929.1:n.*1651C=
ENST00000485852.7:n.489C=
ENST00000497231.7:n.2169C=
ENST00000635851.1:c.1563+1481C=
ENST00000636482.1:n.1276C=
ENST00000636743.1:c.*122C=	ENSP00000489725.1:n.*122C=
ENST00000636808.1:c.*1551C=	ENSP00000490833.1:n.*1551C=
ENST00000636872.1:c.1902C=	ENSP00000490919.1:n.1902C=
ENST00000636879.1:c.*122C=	ENSP00000490811.1:n.*122C=
ENST00000636886.1:c.*122C=	ENSP00000490371.1:n.*122C=
ENST00000637206.1:c.*122C=	ENSP00000489895.1:n.*122C=
ENST00000637272.1:c.*122C=	ENSP00000489686.1:n.*122C=
ENST00000637292.1:c.1198C=
ENST00000637782.1:c.1565+1481C=	ENSP00000490024.1:n.1565+1481C=
ENST00000638008.1:c.*1586C=	ENSP00000490400.1:n.*1586C=
ENST00000638010.1:n.1688C=
ENST00000409134.7:c.*122C=	ENSP00000387123.3:n.*122C=
ENST00000447989.6:c.*122C=	ENSP00000414132.2:n.*122C=
ENST00000485852.6:n.489C=
ENST00000497231.6:n.1952C=
ENST00000553117.5:c.*122C=	ENSP00000448593.1:n.*122C=
NM_001182.4:c.*122C=	NP_001173.2:n.*122C=
NM_001201377.1:c.*122C=	NP_001188306.1:n.*122C=
NM_001202404.1:c.*122C=	NP_001189333.1:n.*122C=
XM_011543417.1:c.*122C=	XP_011541719.1:n.*122C=
XM_011543417.2:c.*122C=	XP_011541719.1:n.*122C=
NM_001182.5:c.*122C= MANE Select	NP_001173.2:n.*122C=
NM_001201377.2:c.*122C=	NP_001188306.1:n.*122C=
NM_001202404.2:c.*122C=	NP_001189333.2:n.*122C=