Canonical Allele Identifier: CA408630176

Gene: SNTA1

Linked Data

• MyVariant Identifiers: chr20:g.31996558A>C (hg19) ; chr20:g.33408752A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33408752A>C , CM000682.2:g.33408752A>C	GRCh38
NC_000020.10:g.31996558A>C , CM000682.1:g.31996558A>C	GRCh37
NC_000020.9:g.31460219A>C	NCBI36
NG_011622.1:g.40141T>G , LRG_332:g.40141T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000217381.3:c.1374T>G MANE Select	ENSP00000217381.2:p.Asp458Glu
ENST00000217381.2:c.1374T>G	ENSP00000217381.2:p.Asp458Glu
NM_003098.2:c.1374T>G , LRG_332t1:c.1374T>G	NP_003089.1:p.Asp458Glu
XM_005260517.1:c.1374T>G	XP_005260574.1:p.Asp458Glu
XM_011529007.1:c.1406T>G	XP_011527309.1:p.Met469Arg
XM_011529008.1:c.1406T>G	XP_011527310.1:p.Met469Arg
XR_936612.1:n.1410T>G
XM_024451971.1:c.1047T>G	XP_024307739.1:p.Asp349Glu
NM_003098.3:c.1374T>G MANE Select	NP_003089.1:p.Asp458Glu