Canonical Allele Identifier: CA714240036

Gene: ALDH1A2

Linked Data

• dbSNP Id: rs1382504368
• gnomAD v3: 15-57987143-A-C
• gnomAD v4: 15-57987143-A-C
• MyVariant Identifiers: chr15:g.58279341A>C (hg19) ; chr15:g.57987143A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.57987143A>C , CM000677.2:g.57987143A>C	GRCh38
NC_000015.9:g.58279341A>C , CM000677.1:g.58279341A>C	GRCh37
NC_000015.8:g.56066633A>C	NCBI36
NG_012259.1:g.83566T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000249750.9:c.798+5562T>G MANE Select	ENSP00000249750.4:n.798+5562T>G
ENST00000249750.8:c.798+5562T>G	ENSP00000249750.4:n.798+5562T>G
ENST00000347587.7:c.684+5802T>G	ENSP00000309623.3:n.684+5802T>G
ENST00000430119.6:c.*772+5562T>G	ENSP00000416754.2:n.*772+5562T>G
ENST00000537372.5:c.735+5562T>G	ENSP00000438296.1:n.735+5562T>G
ENST00000558231.5:c.711+5562T>G	ENSP00000453600.1:n.711+5562T>G
ENST00000559517.5:c.510+5562T>G	ENSP00000453408.1:n.510+5562T>G
NM_001206897.1:c.735+5562T>G	NP_001193826.1:n.735+5562T>G
NM_003888.3:c.798+5562T>G	NP_003879.2:n.798+5562T>G
NM_170696.2:c.684+5802T>G	NP_733797.1:n.684+5802T>G
NM_170697.2:c.510+5562T>G	NP_733798.1:n.510+5562T>G
NM_003888.4:c.798+5562T>G MANE Select	NP_003879.2:n.798+5562T>G
NM_170696.3:c.684+5802T>G	NP_733797.1:n.684+5802T>G
NM_170697.3:c.510+5562T>G	NP_733798.1:n.510+5562T>G
NM_001206897.2:c.735+5562T>G	NP_001193826.1:n.735+5562T>G