Canonical Allele Identifier: CA14119082

Gene: ALDH1A2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.57954718A>G , CM000677.2:g.57954718A>G	GRCh38
NC_000015.9:g.58246916A>G , CM000677.1:g.58246916A>G	GRCh37
NC_000015.8:g.56034208A>G	NCBI36
NG_012259.1:g.115991T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249750.9:c.*479T>C MANE Select	ENSP00000249750.4:n.*479T>C
ENST00000249750.8:c.*479T>C	ENSP00000249750.4:n.*479T>C
ENST00000347587.7:c.*479T>C	ENSP00000309623.3:n.*479T>C
ENST00000430119.6:c.*2010T>C	ENSP00000416754.2:n.*2010T>C
ENST00000537372.5:c.*479T>C	ENSP00000438296.1:n.*479T>C
ENST00000558384.1:c.242+310T>C
ENST00000560312.5:n.1857T>C
NM_001206897.1:c.*479T>C	NP_001193826.1:n.*479T>C
NM_003888.3:c.*479T>C	NP_003879.2:n.*479T>C
NM_170696.2:c.*479T>C	NP_733797.1:n.*479T>C
NM_170697.2:c.*479T>C	NP_733798.1:n.*479T>C
NM_003888.4:c.*479T>C MANE Select	NP_003879.2:n.*479T>C
NM_170696.3:c.*479T>C	NP_733797.1:n.*479T>C
NM_170697.3:c.*479T>C	NP_733798.1:n.*479T>C
NM_001206897.2:c.*479T>C	NP_001193826.1:n.*479T>C