Canonical Allele Identifier: CA510249705
Gene: SNTA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.32000137G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33412331G>A , CM000682.2:g.33412331G>A GRCh38
NC_000020.10:g.32000137G>A , CM000682.1:g.32000137G>A GRCh37
NC_000020.9:g.31463798G>A NCBI36
NG_011622.1:g.36562C>T , LRG_332:g.36562C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000217381.3:c.1005C>T MANE Select ENSP00000217381.2:p.Ser335=
ENST00000217381.2:c.1005C>T ENSP00000217381.2:p.Ser335=
NM_003098.2:c.1005C>T , LRG_332t1:c.1005C>T NP_003089.1:p.Ser335=
XM_005260517.1:c.1005C>T XP_005260574.1:p.Ser335=
XM_011529007.1:c.1005C>T XP_011527309.1:p.Ser335=
XM_011529008.1:c.1005C>T XP_011527310.1:p.Ser335=
XR_936612.1:n.1238C>T
XM_024451971.1:c.678C>T XP_024307739.1:p.Ser226=
NM_003098.3:c.1005C>T MANE Select NP_003089.1:p.Ser335=