Canonical Allele Identifier: CA510252178

Gene: SNTA1

Linked Data

• MyVariant Identifiers: chr20:g.32026678G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33438872G>A , CM000682.2:g.33438872G>A	GRCh38
NC_000020.10:g.32026678G>A , CM000682.1:g.32026678G>A	GRCh37
NC_000020.9:g.31490339G>A	NCBI36
NG_011622.1:g.10021C>T , LRG_332:g.10021C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217381.3:c.465C>T MANE Select	ENSP00000217381.2:p.Leu155=
ENST00000217381.2:c.465C>T	ENSP00000217381.2:p.Leu155=
NM_003098.2:c.465C>T , LRG_332t1:c.465C>T	NP_003089.1:p.Leu155=
XM_005260517.1:c.465C>T	XP_005260574.1:p.Leu155=
XM_011529007.1:c.465C>T	XP_011527309.1:p.Leu155=
XM_011529008.1:c.465C>T	XP_011527310.1:p.Leu155=
XR_936612.1:n.698C>T
XM_024451971.1:c.138C>T	XP_024307739.1:p.Leu46=
NM_003098.3:c.465C>T MANE Select	NP_003089.1:p.Leu155=