Canonical Allele Identifier: CA2652478420
Gene: SNTA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33443593_33443594del , CM000682.2:g.33443593_33443594del GRCh38
NC_000020.10:g.32031399_32031400del , CM000682.1:g.32031399_32031400del GRCh37
NC_000020.9:g.31495060_31495061del NCBI36
NG_011622.1:g.5300_5301del , LRG_332:g.5300_5301del

Transcript Alleles

HGVS Amino-acid Change
ENST00000217381.3:c.28_29del MANE Select ENSP00000217381.2:p.Thr10ArgfsTer?
ENST00000217381.2:c.28_29del ENSP00000217381.2:p.Thr10ArgfsTer?
NM_003098.2:c.28_29del , LRG_332t1:c.28_29del NP_003089.1:p.Thr10ArgfsTer?
XM_005260517.1:c.28_29del XP_005260574.1:p.Thr10ArgfsTer?
XM_011529007.1:c.28_29del XP_011527309.1:p.Thr10ArgfsTer?
XM_011529008.1:c.28_29del XP_011527310.1:p.Thr10ArgfsTer?
XR_936612.1:n.261_262del
NM_003098.3:c.28_29del MANE Select NP_003089.1:p.Thr10ArgfsTer?