Canonical Allele Identifier: CA360717836

Gene: ALDH7A1

Linked Data

• MyVariant Identifiers: chr5:g.125880695T>G (hg19) ; chr5:g.126545003T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.126545003T>G , CM000667.2:g.126545003T>G	GRCh38
NC_000005.9:g.125880695T>G , CM000667.1:g.125880695T>G	GRCh37
NC_000005.8:g.125908594T>G	NCBI36
NG_008600.2:g.55388A>C
NG_008600.3:g.55388A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409134.8:c.1582A>C MANE Select	ENSP00000387123.3:p.Lys528Gln
ENST00000458249.6:c.*1491A>C	ENSP00000403929.1:n.*1491A>C
ENST00000485852.7:n.329A>C
ENST00000497231.7:n.2009A>C
ENST00000635851.1:c.1563+1321A>C
ENST00000636286.1:n.1347A>C
ENST00000636482.1:n.1116A>C
ENST00000636743.1:c.1462A>C	ENSP00000489725.1:p.Lys488Gln
ENST00000636808.1:c.*1391A>C	ENSP00000490833.1:n.*1391A>C
ENST00000636872.1:c.1742A>C	ENSP00000490919.1:n.1742A>C
ENST00000636879.1:c.1627A>C	ENSP00000490811.1:p.Lys543Gln
ENST00000636886.1:c.1381A>C	ENSP00000490371.1:p.Lys461Gln
ENST00000637206.1:c.1402A>C	ENSP00000489895.1:p.Lys468Gln
ENST00000637272.1:c.1573A>C	ENSP00000489686.1:p.Lys525Gln
ENST00000637292.1:c.1038A>C
ENST00000637782.1:c.1565+1321A>C	ENSP00000490024.1:n.1565+1321A>C
ENST00000638008.1:c.*1426A>C	ENSP00000490400.1:n.*1426A>C
ENST00000638010.1:n.1528A>C
ENST00000409134.7:c.1582A>C	ENSP00000387123.3:p.Lys528Gln
ENST00000447989.6:c.1471A>C	ENSP00000414132.2:p.Lys491Gln
ENST00000485852.6:n.329A>C
ENST00000497231.6:n.1792A>C
ENST00000553117.5:c.1390A>C	ENSP00000448593.1:p.Lys464Gln
NM_001182.4:c.1582A>C	NP_001173.2:p.Lys528Gln
NM_001201377.1:c.1498A>C	NP_001188306.1:p.Lys500Gln
NM_001202404.1:c.1471A>C	NP_001189333.1:p.Lys491Gln
XM_011543417.1:c.1177A>C	XP_011541719.1:p.Lys393Gln
XM_011543417.2:c.1177A>C	XP_011541719.1:p.Lys393Gln
NM_001182.5:c.1582A>C MANE Select	NP_001173.2:p.Lys528Gln
NM_001201377.2:c.1498A>C	NP_001188306.1:p.Lys500Gln
NM_001202404.2:c.1390A>C	NP_001189333.2:p.Lys464Gln