Canonical Allele Identifier: CA2652478413
Gene: SNTA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33443564del , CM000682.2:g.33443564del GRCh38
NC_000020.10:g.32031370del , CM000682.1:g.32031370del GRCh37
NC_000020.9:g.31495031del NCBI36
NG_011622.1:g.5331del , LRG_332:g.5331del

Transcript Alleles

HGVS Amino-acid Change
ENST00000217381.3:c.59del MANE Select ENSP00000217381.2:p.Gly20AlafsTer14
ENST00000217381.2:c.59del ENSP00000217381.2:p.Gly20AlafsTer14
NM_003098.2:c.59del , LRG_332t1:c.59del NP_003089.1:p.Gly20AlafsTer14
XM_005260517.1:c.59del XP_005260574.1:p.Gly20AlafsTer14
XM_011529007.1:c.59del XP_011527309.1:p.Gly20AlafsTer14
XM_011529008.1:c.59del XP_011527310.1:p.Gly20AlafsTer14
XR_936612.1:n.292del
NM_003098.3:c.59del MANE Select NP_003089.1:p.Gly20AlafsTer14