Canonical Allele Identifier: CA1017044260
Gene: SNTA1 HGNC NCBI

Linked Data

dbSNP Id: rs1990644019

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33443801del , CM000682.2:g.33443801del GRCh38
NC_000020.10:g.32031607del , CM000682.1:g.32031607del GRCh37
NC_000020.9:g.31495268del NCBI36
NG_011622.1:g.5095del , LRG_332:g.5095del

Transcript Alleles

HGVS Amino-acid Change
ENST00000217381.2:c.-178del ENSP00000217381.2:n.-178del
NM_003098.2:c.-178del , LRG_332t1:c.-178del NP_003089.1:n.-178del
XM_005260517.1:c.-178del XP_005260574.1:n.-178del
XM_011529007.1:c.-178del XP_011527309.1:n.-178del
XM_011529008.1:c.-178del XP_011527310.1:n.-178del
XR_936612.1:n.56del