Canonical Allele Identifier: CA2360755166
Gene: SNTA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33443797_33443798delinsTG , CM000682.2:g.33443797_33443798delinsTG GRCh38
NC_000020.10:g.32031603_32031604delinsTG , CM000682.1:g.32031603_32031604delinsTG GRCh37
NC_000020.9:g.31495264_31495265delinsTG NCBI36
NG_011622.1:g.5095_5096delinsCA , LRG_332:g.5095_5096delinsCA

Transcript Alleles

HGVS Amino-acid change
ENST00000217381.2:c.-178_-177delinsCA ENSP00000217381.2:n.-178_-177delinsCA
NM_003098.2:c.-178_-177delinsCA , LRG_332t1:c.-178_-177delinsCA NP_003089.1:n.-178_-177delinsCA
XM_005260517.1:c.-178_-177delinsCA XP_005260574.1:n.-178_-177delinsCA
XM_011529007.1:c.-178_-177delinsCA XP_011527309.1:n.-178_-177delinsCA
XM_011529008.1:c.-178_-177delinsCA XP_011527310.1:n.-178_-177delinsCA
XR_936612.1:n.56_57delinsCA