Canonical Allele Identifier: CA360733136

Gene: ALDH7A1

Linked Data

• MyVariant Identifiers: chr5:g.125928387T>C (hg19) ; chr5:g.126592695T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.126592695T>C , CM000667.2:g.126592695T>C	GRCh38
NC_000005.9:g.125928387T>C , CM000667.1:g.125928387T>C	GRCh37
NC_000005.8:g.125956286T>C	NCBI36
NG_008600.2:g.7696A>G
NG_008600.3:g.7696A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409134.8:c.281A>G MANE Select	ENSP00000387123.3:p.Lys94Arg
ENST00000412186.2:c.281A>G	ENSP00000414536.2:p.Lys94Arg
ENST00000413020.6:c.281A>G	ENSP00000487936.1:p.Lys94Arg
ENST00000458249.6:c.*190A>G	ENSP00000403929.1:n.*190A>G
ENST00000479989.6:n.464A>G
ENST00000503281.6:c.106+2312A>G
ENST00000509270.2:c.246+656A>G	ENSP00000449318.2:n.246+656A>G
ENST00000509459.6:c.65+2312A>G
ENST00000511266.6:n.1003A>G
ENST00000635851.1:c.279A>G
ENST00000635858.1:n.120A>G
ENST00000635933.1:n.310A>G
ENST00000636062.1:n.176A>G
ENST00000636190.1:n.160A>G
ENST00000636225.1:c.*90A>G	ENSP00000490797.1:n.*90A>G
ENST00000636743.1:c.192+2312A>G	ENSP00000489725.1:n.192+2312A>G
ENST00000636808.1:c.*90A>G	ENSP00000490833.1:n.*90A>G
ENST00000636872.1:c.441A>G	ENSP00000490919.1:n.441A>G
ENST00000636879.1:c.281A>G	ENSP00000490811.1:p.Lys94Arg
ENST00000636886.1:c.192+2312A>G	ENSP00000490371.1:n.192+2312A>G
ENST00000637206.1:c.281A>G	ENSP00000489895.1:p.Lys94Arg
ENST00000637272.1:c.281A>G	ENSP00000489686.1:p.Lys94Arg
ENST00000637782.1:c.281A>G	ENSP00000490024.1:p.Lys94Arg
ENST00000637964.1:c.227A>G	ENSP00000490291.1:p.Lys76Arg
ENST00000638008.1:c.*90A>G	ENSP00000490400.1:n.*90A>G
ENST00000409134.7:c.281A>G	ENSP00000387123.3:p.Lys94Arg
ENST00000412186.1:c.*90A>G	ENSP00000414536.1:n.*90A>G
ENST00000413020.5:c.281A>G	ENSP00000487936.1:p.Lys94Arg
ENST00000447989.6:c.362A>G	ENSP00000414132.2:p.Lys121Arg
ENST00000458249.5:c.441A>G	ENSP00000403929.1:n.441A>G
ENST00000479989.5:n.464A>G
ENST00000503281.5:c.106+2312A>G
ENST00000509270.1:c.192+2312A>G	ENSP00000449318.1:n.192+2312A>G
ENST00000509459.5:c.65+2312A>G
ENST00000510111.6:c.275A>G	ENSP00000447388.1:p.Lys92Arg
ENST00000511266.5:n.236A>G
ENST00000553117.5:c.281A>G	ENSP00000448593.1:p.Lys94Arg
NM_001182.4:c.281A>G	NP_001173.2:p.Lys94Arg
NM_001201377.1:c.197A>G	NP_001188306.1:p.Lys66Arg
NM_001202404.1:c.362A>G	NP_001189333.1:p.Lys121Arg
XM_011543417.1:c.-125A>G	XP_011541719.1:n.-125A>G
XM_011543417.2:c.-125A>G	XP_011541719.1:n.-125A>G
NM_001182.5:c.281A>G MANE Select	NP_001173.2:p.Lys94Arg
NM_001201377.2:c.197A>G	NP_001188306.1:p.Lys66Arg
NM_001202404.2:c.281A>G	NP_001189333.2:p.Lys94Arg