Canonical Allele Identifier: CA408633371

Gene: SNTA1

Linked Data

• dbSNP Id: rs1990508824
• MyVariant Identifiers: chr20:g.32026685T>G (hg19) ; chr20:g.33438879T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33438879T>G , CM000682.2:g.33438879T>G	GRCh38
NC_000020.10:g.32026685T>G , CM000682.1:g.32026685T>G	GRCh37
NC_000020.9:g.31490346T>G	NCBI36
NG_011622.1:g.10014A>C , LRG_332:g.10014A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217381.3:c.458A>C MANE Select	ENSP00000217381.2:p.Gln153Pro
ENST00000217381.2:c.458A>C	ENSP00000217381.2:p.Gln153Pro
NM_003098.2:c.458A>C , LRG_332t1:c.458A>C	NP_003089.1:p.Gln153Pro
XM_005260517.1:c.458A>C	XP_005260574.1:p.Gln153Pro
XM_011529007.1:c.458A>C	XP_011527309.1:p.Gln153Pro
XM_011529008.1:c.458A>C	XP_011527310.1:p.Gln153Pro
XR_936612.1:n.691A>C
XM_024451971.1:c.131A>C	XP_024307739.1:p.Gln44Pro
NM_003098.3:c.458A>C MANE Select	NP_003089.1:p.Gln153Pro