Canonical Allele Identifier: CA360717704

Gene: ALDH7A1

Linked Data

• MyVariant Identifiers: chr5:g.125880682A>G (hg19) ; chr5:g.126544990A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.126544990A>G , CM000667.2:g.126544990A>G	GRCh38
NC_000005.9:g.125880682A>G , CM000667.1:g.125880682A>G	GRCh37
NC_000005.8:g.125908581A>G	NCBI36
NG_008600.2:g.55401T>C
NG_008600.3:g.55401T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409134.8:c.1595T>C MANE Select	ENSP00000387123.3:p.Leu532Pro
ENST00000458249.6:c.*1504T>C	ENSP00000403929.1:n.*1504T>C
ENST00000485852.7:n.342T>C
ENST00000497231.7:n.2022T>C
ENST00000635851.1:c.1563+1334T>C
ENST00000636286.1:n.1360T>C
ENST00000636482.1:n.1129T>C
ENST00000636743.1:c.1475T>C	ENSP00000489725.1:p.Leu492Pro
ENST00000636808.1:c.*1404T>C	ENSP00000490833.1:n.*1404T>C
ENST00000636872.1:c.1755T>C	ENSP00000490919.1:n.1755T>C
ENST00000636879.1:c.1640T>C	ENSP00000490811.1:p.Leu547Pro
ENST00000636886.1:c.1394T>C	ENSP00000490371.1:p.Leu465Pro
ENST00000637206.1:c.1415T>C	ENSP00000489895.1:p.Leu472Pro
ENST00000637272.1:c.1586T>C	ENSP00000489686.1:p.Leu529Pro
ENST00000637292.1:c.1051T>C
ENST00000637782.1:c.1565+1334T>C	ENSP00000490024.1:n.1565+1334T>C
ENST00000638008.1:c.*1439T>C	ENSP00000490400.1:n.*1439T>C
ENST00000638010.1:n.1541T>C
ENST00000409134.7:c.1595T>C	ENSP00000387123.3:p.Leu532Pro
ENST00000447989.6:c.1484T>C	ENSP00000414132.2:p.Leu495Pro
ENST00000485852.6:n.342T>C
ENST00000497231.6:n.1805T>C
ENST00000553117.5:c.1403T>C	ENSP00000448593.1:p.Leu468Pro
NM_001182.4:c.1595T>C	NP_001173.2:p.Leu532Pro
NM_001201377.1:c.1511T>C	NP_001188306.1:p.Leu504Pro
NM_001202404.1:c.1484T>C	NP_001189333.1:p.Leu495Pro
XM_011543417.1:c.1190T>C	XP_011541719.1:p.Leu397Pro
XM_011543417.2:c.1190T>C	XP_011541719.1:p.Leu397Pro
NM_001182.5:c.1595T>C MANE Select	NP_001173.2:p.Leu532Pro
NM_001201377.2:c.1511T>C	NP_001188306.1:p.Leu504Pro
NM_001202404.2:c.1403T>C	NP_001189333.2:p.Leu468Pro