Canonical Allele Identifier: CA408630156

Gene: SNTA1

Linked Data

• MyVariant Identifiers: chr20:g.31996548T>C (hg19) ; chr20:g.33408742T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33408742T>C , CM000682.2:g.33408742T>C	GRCh38
NC_000020.10:g.31996548T>C , CM000682.1:g.31996548T>C	GRCh37
NC_000020.9:g.31460209T>C	NCBI36
NG_011622.1:g.40151A>G , LRG_332:g.40151A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000217381.3:c.1384A>G MANE Select	ENSP00000217381.2:p.Ser462Gly
ENST00000217381.2:c.1384A>G	ENSP00000217381.2:p.Ser462Gly
NM_003098.2:c.1384A>G , LRG_332t1:c.1384A>G	NP_003089.1:p.Ser462Gly
XM_005260517.1:c.1384A>G	XP_005260574.1:p.Ser462Gly
XM_011529007.1:c.1416A>G	XP_011527309.1:p.Pro472=
XM_011529008.1:c.1416A>G	XP_011527310.1:p.Pro472=
XR_936612.1:n.1420A>G
XM_024451971.1:c.1057A>G	XP_024307739.1:p.Ser353Gly
NM_003098.3:c.1384A>G MANE Select	NP_003089.1:p.Ser462Gly