Canonical Allele Identifier: CA393949406

Gene: ALDH1A3 ALDH1A3-AS1

Linked Data

• dbSNP Id: rs2041913579
• gnomAD v4: 15-100914744-A-T
• MyVariant Identifiers: chr15:g.101454949A>T (hg19) ; chr15:g.100914744A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.100914744A>T , CM000677.2:g.100914744A>T	GRCh38
NC_000015.9:g.101454949A>T , CM000677.1:g.101454949A>T	GRCh37
NC_000015.8:g.99272472A>T	NCBI36
NG_012254.1:g.39941A>T
NG_052791.1:g.728A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329841.10:c.1510A>T (ALDH1A3) MANE Select	ENSP00000332256.5:p.Thr504Ser
ENST00000329841.9:c.1510A>T (ALDH1A3)	ENSP00000332256.5:p.Thr504Ser
ENST00000346623.6:c.1189A>T (ALDH1A3)	ENSP00000343294.6:p.Thr397Ser
NM_000693.3:c.1510A>T (ALDH1A3)	NP_000684.2:p.Thr504Ser
NM_001293815.1:c.1189A>T (ALDH1A3)	NP_001280744.1:p.Thr397Ser
NR_135827.1:n.480+4060T>A (ALDH1A3-AS1)
NR_135828.1:n.1717T>A (ALDH1A3-AS1)
NR_135831.1:n.2633T>A (ALDH1A3-AS1)
NM_000693.4:c.1510A>T (ALDH1A3) MANE Select	NP_000684.2:p.Thr504Ser
NM_001293815.2:c.1189A>T (ALDH1A3)	NP_001280744.1:p.Thr397Ser