Canonical Allele Identifier: CA1580460343

Gene: ALDH7A1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.126592670C= , CM000667.2:g.126592670C=	GRCh38
NC_000005.9:g.125928362C= , CM000667.1:g.125928362C=	GRCh37
NC_000005.8:g.125956261C=	NCBI36
NG_008600.2:g.7721G=
NG_008600.3:g.7721G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000409134.8:c.306G= MANE Select	ENSP00000387123.3:p.Trp102=
ENST00000412186.2:c.306G=	ENSP00000414536.2:p.Trp102=
ENST00000413020.6:c.306G=	ENSP00000487936.1:p.Trp102=
ENST00000458249.6:c.*215G=	ENSP00000403929.1:n.*215G=
ENST00000479989.6:n.489G=
ENST00000503281.6:c.106+2337G=
ENST00000509270.2:c.246+681G=	ENSP00000449318.2:n.246+681G=
ENST00000509459.6:c.65+2337G=
ENST00000511266.6:n.1028G=
ENST00000635851.1:c.304G=
ENST00000635858.1:n.145G=
ENST00000635933.1:n.335G=
ENST00000636062.1:n.201G=
ENST00000636190.1:n.185G=
ENST00000636225.1:c.*115G=	ENSP00000490797.1:n.*115G=
ENST00000636743.1:c.192+2337G=	ENSP00000489725.1:n.192+2337G=
ENST00000636808.1:c.*115G=	ENSP00000490833.1:n.*115G=
ENST00000636872.1:c.466G=	ENSP00000490919.1:n.466G=
ENST00000636879.1:c.306G=	ENSP00000490811.1:p.Trp102=
ENST00000636886.1:c.192+2337G=	ENSP00000490371.1:n.192+2337G=
ENST00000637206.1:c.306G=	ENSP00000489895.1:p.Trp102=
ENST00000637272.1:c.306G=	ENSP00000489686.1:p.Trp102=
ENST00000637782.1:c.306G=	ENSP00000490024.1:p.Trp102=
ENST00000637964.1:c.252G=	ENSP00000490291.1:p.Trp84=
ENST00000638008.1:c.*115G=	ENSP00000490400.1:n.*115G=
ENST00000409134.7:c.306G=	ENSP00000387123.3:p.Trp102=
ENST00000412186.1:c.*115G=	ENSP00000414536.1:n.*115G=
ENST00000413020.5:c.306G=	ENSP00000487936.1:p.Trp102=
ENST00000447989.6:c.387G=	ENSP00000414132.2:p.Trp129=
ENST00000458249.5:c.466G=	ENSP00000403929.1:n.466G=
ENST00000479989.5:n.489G=
ENST00000503281.5:c.106+2337G=
ENST00000509270.1:c.192+2337G=	ENSP00000449318.1:n.192+2337G=
ENST00000509459.5:c.65+2337G=
ENST00000510111.6:c.300G=	ENSP00000447388.1:p.Trp100=
ENST00000511266.5:n.261G=
ENST00000553117.5:c.306G=	ENSP00000448593.1:p.Trp102=
NM_001182.4:c.306G=	NP_001173.2:p.Trp102=
NM_001201377.1:c.222G=	NP_001188306.1:p.Trp74=
NM_001202404.1:c.387G=	NP_001189333.1:p.Trp129=
XM_011543417.1:c.-100G=	XP_011541719.1:n.-100G=
XM_011543417.2:c.-100G=	XP_011541719.1:n.-100G=
NM_001182.5:c.306G= MANE Select	NP_001173.2:p.Trp102=
NM_001201377.2:c.222G=	NP_001188306.1:p.Trp74=
NM_001202404.2:c.306G=	NP_001189333.2:p.Trp102=