Canonical Allele Identifier: CA1580440312

Gene: ALDH7A1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.126544787T= , CM000667.2:g.126544787T=	GRCh38
NC_000005.9:g.125880479T= , CM000667.1:g.125880479T=	GRCh37
NC_000005.8:g.125908378T=	NCBI36
NG_008600.2:g.55604A=
NG_008600.3:g.55604A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409134.8:c.*178A= MANE Select	ENSP00000387123.3:n.*178A=
ENST00000458249.6:c.*1707A=	ENSP00000403929.1:n.*1707A=
ENST00000485852.7:n.545A=
ENST00000497231.7:n.2225A=
ENST00000635851.1:c.1563+1537A=
ENST00000636482.1:n.1332A=
ENST00000636743.1:c.*178A=	ENSP00000489725.1:n.*178A=
ENST00000636808.1:c.*1607A=	ENSP00000490833.1:n.*1607A=
ENST00000636872.1:c.1958A=	ENSP00000490919.1:n.1958A=
ENST00000636879.1:c.*178A=	ENSP00000490811.1:n.*178A=
ENST00000636886.1:c.*178A=	ENSP00000490371.1:n.*178A=
ENST00000637206.1:c.*178A=	ENSP00000489895.1:n.*178A=
ENST00000637272.1:c.*178A=	ENSP00000489686.1:n.*178A=
ENST00000637782.1:c.1565+1537A=	ENSP00000490024.1:n.1565+1537A=
ENST00000638010.1:n.1744A=
ENST00000409134.7:c.*178A=	ENSP00000387123.3:n.*178A=
ENST00000447989.6:c.*178A=	ENSP00000414132.2:n.*178A=
ENST00000485852.6:n.545A=
ENST00000497231.6:n.2008A=
ENST00000553117.5:c.*178A=	ENSP00000448593.1:n.*178A=
NM_001182.4:c.*178A=	NP_001173.2:n.*178A=
NM_001201377.1:c.*178A=	NP_001188306.1:n.*178A=
NM_001202404.1:c.*178A=	NP_001189333.1:n.*178A=
XM_011543417.1:c.*178A=	XP_011541719.1:n.*178A=
XM_011543417.2:c.*178A=	XP_011541719.1:n.*178A=
NM_001182.5:c.*178A= MANE Select	NP_001173.2:n.*178A=
NM_001201377.2:c.*178A=	NP_001188306.1:n.*178A=
NM_001202404.2:c.*178A=	NP_001189333.2:n.*178A=