Canonical Allele Identifier: CA271343876

Gene: ALDH1A2

Linked Data

• dbSNP Id: rs751828838
• MyVariant Identifiers: chr15:g.58279454del (hg19) ; chr15:g.57987256del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.57987256del , CM000677.2:g.57987256del	GRCh38
NC_000015.9:g.58279454del , CM000677.1:g.58279454del	GRCh37
NC_000015.8:g.56066746del	NCBI36
NG_012259.1:g.83453del

Transcript Alleles

HGVS	Amino-acid change
ENST00000249750.9:c.798+5449del MANE Select	ENSP00000249750.4:n.798+5449del
ENST00000249750.8:c.798+5449del	ENSP00000249750.4:n.798+5449del
ENST00000347587.7:c.684+5689del	ENSP00000309623.3:n.684+5689del
ENST00000430119.6:c.*772+5449del	ENSP00000416754.2:n.*772+5449del
ENST00000537372.5:c.735+5449del	ENSP00000438296.1:n.735+5449del
ENST00000558231.5:c.711+5449del	ENSP00000453600.1:n.711+5449del
ENST00000559517.5:c.510+5449del	ENSP00000453408.1:n.510+5449del
NM_001206897.1:c.735+5449del	NP_001193826.1:n.735+5449del
NM_003888.3:c.798+5449del	NP_003879.2:n.798+5449del
NM_170696.2:c.684+5689del	NP_733797.1:n.684+5689del
NM_170697.2:c.510+5449del	NP_733798.1:n.510+5449del
NM_003888.4:c.798+5449del MANE Select	NP_003879.2:n.798+5449del
NM_170696.3:c.684+5689del	NP_733797.1:n.684+5689del
NM_170697.3:c.510+5449del	NP_733798.1:n.510+5449del
NM_001206897.2:c.735+5449del	NP_001193826.1:n.735+5449del