Canonical Allele Identifier: CA393949247

Gene: ALDH1A3 ALDH1A3-AS1

Linked Data

• dbSNP Id: rs1310945145
• gnomAD v2: 15-101454914-A-G
• gnomAD v4: 15-100914709-A-G
• MyVariant Identifiers: chr15:g.101454914A>G (hg19) ; chr15:g.100914709A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.100914709A>G , CM000677.2:g.100914709A>G	GRCh38
NC_000015.9:g.101454914A>G , CM000677.1:g.101454914A>G	GRCh37
NC_000015.8:g.99272437A>G	NCBI36
NG_012254.1:g.39906A>G
NG_052791.1:g.693A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329841.10:c.1475A>G (ALDH1A3) MANE Select	ENSP00000332256.5:p.Tyr492Cys
ENST00000329841.9:c.1475A>G (ALDH1A3)	ENSP00000332256.5:p.Tyr492Cys
ENST00000346623.6:c.1154A>G (ALDH1A3)	ENSP00000343294.6:p.Tyr385Cys
NM_000693.3:c.1475A>G (ALDH1A3)	NP_000684.2:p.Tyr492Cys
NM_001293815.1:c.1154A>G (ALDH1A3)	NP_001280744.1:p.Tyr385Cys
NR_135827.1:n.480+4095T>C (ALDH1A3-AS1)
NR_135828.1:n.1752T>C (ALDH1A3-AS1)
NR_135831.1:n.2668T>C (ALDH1A3-AS1)
NM_000693.4:c.1475A>G (ALDH1A3) MANE Select	NP_000684.2:p.Tyr492Cys
NM_001293815.2:c.1154A>G (ALDH1A3)	NP_001280744.1:p.Tyr385Cys