Canonical Allele Identifier: CA393949331

Gene: ALDH1A3 ALDH1A3-AS1

Linked Data

• dbSNP Id: rs1168265416
• gnomAD v2: 15-101454932-C-T
• gnomAD v4: 15-100914727-C-T
• MyVariant Identifiers: chr15:g.101454932C>T (hg19) ; chr15:g.100914727C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.100914727C>T , CM000677.2:g.100914727C>T	GRCh38
NC_000015.9:g.101454932C>T , CM000677.1:g.101454932C>T	GRCh37
NC_000015.8:g.99272455C>T	NCBI36
NG_012254.1:g.39924C>T
NG_052791.1:g.711C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329841.10:c.1493C>T (ALDH1A3) MANE Select	ENSP00000332256.5:p.Thr498Ile
ENST00000329841.9:c.1493C>T (ALDH1A3)	ENSP00000332256.5:p.Thr498Ile
ENST00000346623.6:c.1172C>T (ALDH1A3)	ENSP00000343294.6:p.Thr391Ile
NM_000693.3:c.1493C>T (ALDH1A3)	NP_000684.2:p.Thr498Ile
NM_001293815.1:c.1172C>T (ALDH1A3)	NP_001280744.1:p.Thr391Ile
NR_135827.1:n.480+4077G>A (ALDH1A3-AS1)
NR_135828.1:n.1734G>A (ALDH1A3-AS1)
NR_135831.1:n.2650G>A (ALDH1A3-AS1)
NM_000693.4:c.1493C>T (ALDH1A3) MANE Select	NP_000684.2:p.Thr498Ile
NM_001293815.2:c.1172C>T (ALDH1A3)	NP_001280744.1:p.Thr391Ile