Canonical Allele Identifier: CA408633568

Gene: SNTA1

Linked Data

• MyVariant Identifiers: chr20:g.32026779C>A (hg19) ; chr20:g.33438973C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33438973C>A , CM000682.2:g.33438973C>A	GRCh38
NC_000020.10:g.32026779C>A , CM000682.1:g.32026779C>A	GRCh37
NC_000020.9:g.31490440C>A	NCBI36
NG_011622.1:g.9920G>T , LRG_332:g.9920G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217381.3:c.364G>T MANE Select	ENSP00000217381.2:p.Ala122Ser
ENST00000217381.2:c.364G>T	ENSP00000217381.2:p.Ala122Ser
NM_003098.2:c.364G>T , LRG_332t1:c.364G>T	NP_003089.1:p.Ala122Ser
XM_005260517.1:c.364G>T	XP_005260574.1:p.Ala122Ser
XM_011529007.1:c.364G>T	XP_011527309.1:p.Ala122Ser
XM_011529008.1:c.364G>T	XP_011527310.1:p.Ala122Ser
XR_936612.1:n.597G>T
XM_024451971.1:c.37G>T	XP_024307739.1:p.Ala13Ser
NM_003098.3:c.364G>T MANE Select	NP_003089.1:p.Ala122Ser