Canonical Allele Identifier: CA408633517

Gene: SNTA1

Linked Data

• MyVariant Identifiers: chr20:g.32026755A>C (hg19) ; chr20:g.33438949A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33438949A>C , CM000682.2:g.33438949A>C	GRCh38
NC_000020.10:g.32026755A>C , CM000682.1:g.32026755A>C	GRCh37
NC_000020.9:g.31490416A>C	NCBI36
NG_011622.1:g.9944T>G , LRG_332:g.9944T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217381.3:c.388T>G MANE Select	ENSP00000217381.2:p.Phe130Val
ENST00000217381.2:c.388T>G	ENSP00000217381.2:p.Phe130Val
NM_003098.2:c.388T>G , LRG_332t1:c.388T>G	NP_003089.1:p.Phe130Val
XM_005260517.1:c.388T>G	XP_005260574.1:p.Phe130Val
XM_011529007.1:c.388T>G	XP_011527309.1:p.Phe130Val
XM_011529008.1:c.388T>G	XP_011527310.1:p.Phe130Val
XR_936612.1:n.621T>G
XM_024451971.1:c.61T>G	XP_024307739.1:p.Phe21Val
NM_003098.3:c.388T>G MANE Select	NP_003089.1:p.Phe130Val