Canonical Allele Identifier: CA360733157

Gene: ALDH7A1

Linked Data

• MyVariant Identifiers: chr5:g.125928396G>C (hg19) ; chr5:g.126592704G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.126592704G>C , CM000667.2:g.126592704G>C	GRCh38
NC_000005.9:g.125928396G>C , CM000667.1:g.125928396G>C	GRCh37
NC_000005.8:g.125956295G>C	NCBI36
NG_008600.2:g.7687C>G
NG_008600.3:g.7687C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409134.8:c.272C>G MANE Select	ENSP00000387123.3:p.Thr91Ser
ENST00000412186.2:c.272C>G	ENSP00000414536.2:p.Thr91Ser
ENST00000413020.6:c.272C>G	ENSP00000487936.1:p.Thr91Ser
ENST00000458249.6:c.*181C>G	ENSP00000403929.1:n.*181C>G
ENST00000479989.6:n.455C>G
ENST00000503281.6:c.106+2303C>G
ENST00000509270.2:c.246+647C>G	ENSP00000449318.2:n.246+647C>G
ENST00000509459.6:c.65+2303C>G
ENST00000511266.6:n.994C>G
ENST00000635851.1:c.270C>G
ENST00000635858.1:n.111C>G
ENST00000635933.1:n.301C>G
ENST00000636062.1:n.167C>G
ENST00000636190.1:n.151C>G
ENST00000636225.1:c.*81C>G	ENSP00000490797.1:n.*81C>G
ENST00000636743.1:c.192+2303C>G	ENSP00000489725.1:n.192+2303C>G
ENST00000636808.1:c.*81C>G	ENSP00000490833.1:n.*81C>G
ENST00000636872.1:c.432C>G	ENSP00000490919.1:n.432C>G
ENST00000636879.1:c.272C>G	ENSP00000490811.1:p.Thr91Ser
ENST00000636886.1:c.192+2303C>G	ENSP00000490371.1:n.192+2303C>G
ENST00000637206.1:c.272C>G	ENSP00000489895.1:p.Thr91Ser
ENST00000637272.1:c.272C>G	ENSP00000489686.1:p.Thr91Ser
ENST00000637782.1:c.272C>G	ENSP00000490024.1:p.Thr91Ser
ENST00000637964.1:c.218C>G	ENSP00000490291.1:p.Thr73Ser
ENST00000638008.1:c.*81C>G	ENSP00000490400.1:n.*81C>G
ENST00000409134.7:c.272C>G	ENSP00000387123.3:p.Thr91Ser
ENST00000412186.1:c.*81C>G	ENSP00000414536.1:n.*81C>G
ENST00000413020.5:c.272C>G	ENSP00000487936.1:p.Thr91Ser
ENST00000447989.6:c.353C>G	ENSP00000414132.2:p.Thr118Ser
ENST00000458249.5:c.432C>G	ENSP00000403929.1:n.432C>G
ENST00000479989.5:n.455C>G
ENST00000503281.5:c.106+2303C>G
ENST00000509270.1:c.192+2303C>G	ENSP00000449318.1:n.192+2303C>G
ENST00000509459.5:c.65+2303C>G
ENST00000510111.6:c.266C>G	ENSP00000447388.1:p.Thr89Ser
ENST00000511266.5:n.227C>G
ENST00000553117.5:c.272C>G	ENSP00000448593.1:p.Thr91Ser
NM_001182.4:c.272C>G	NP_001173.2:p.Thr91Ser
NM_001201377.1:c.188C>G	NP_001188306.1:p.Thr63Ser
NM_001202404.1:c.353C>G	NP_001189333.1:p.Thr118Ser
XM_011543417.1:c.-134C>G	XP_011541719.1:n.-134C>G
XM_011543417.2:c.-134C>G	XP_011541719.1:n.-134C>G
NM_001182.5:c.272C>G MANE Select	NP_001173.2:p.Thr91Ser
NM_001201377.2:c.188C>G	NP_001188306.1:p.Thr63Ser
NM_001202404.2:c.272C>G	NP_001189333.2:p.Thr91Ser