Canonical Allele Identifier: CA408633349
Gene: SNTA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33438869C>A , CM000682.2:g.33438869C>A GRCh38
NC_000020.10:g.32026675C>A , CM000682.1:g.32026675C>A GRCh37
NC_000020.9:g.31490336C>A NCBI36
NG_011622.1:g.10024G>T , LRG_332:g.10024G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000217381.3:c.468G>T MANE Select ENSP00000217381.2:p.Lys156Asn
ENST00000217381.2:c.468G>T ENSP00000217381.2:p.Lys156Asn
NM_003098.2:c.468G>T , LRG_332t1:c.468G>T NP_003089.1:p.Lys156Asn
XM_005260517.1:c.468G>T XP_005260574.1:p.Lys156Asn
XM_011529007.1:c.468G>T XP_011527309.1:p.Lys156Asn
XM_011529008.1:c.468G>T XP_011527310.1:p.Lys156Asn
XR_936612.1:n.701G>T
XM_024451971.1:c.141G>T XP_024307739.1:p.Lys47Asn
NM_003098.3:c.468G>T MANE Select NP_003089.1:p.Lys156Asn