Canonical Allele Identifier: CA408633348
Gene: SNTA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33438868T>G , CM000682.2:g.33438868T>G GRCh38
NC_000020.10:g.32026674T>G , CM000682.1:g.32026674T>G GRCh37
NC_000020.9:g.31490335T>G NCBI36
NG_011622.1:g.10025A>C , LRG_332:g.10025A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000217381.3:c.469A>C MANE Select ENSP00000217381.2:p.Lys157Gln
ENST00000217381.2:c.469A>C ENSP00000217381.2:p.Lys157Gln
NM_003098.2:c.469A>C , LRG_332t1:c.469A>C NP_003089.1:p.Lys157Gln
XM_005260517.1:c.469A>C XP_005260574.1:p.Lys157Gln
XM_011529007.1:c.469A>C XP_011527309.1:p.Lys157Gln
XM_011529008.1:c.469A>C XP_011527310.1:p.Lys157Gln
XR_936612.1:n.702A>C
XM_024451971.1:c.142A>C XP_024307739.1:p.Lys48Gln
NM_003098.3:c.469A>C MANE Select NP_003089.1:p.Lys157Gln