Canonical Allele Identifier: CA2577372614
Gene: SNTA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33417917del , CM000682.2:g.33417917del GRCh38
NC_000020.10:g.32005723del , CM000682.1:g.32005723del GRCh37
NC_000020.9:g.31469384del NCBI36
NG_011622.1:g.30976del , LRG_332:g.30976del

Transcript Alleles

HGVS Amino-acid Change
ENST00000217381.3:c.503del MANE Select ENSP00000217381.2:p.Tyr168LeufsTer2
ENST00000217381.2:c.503del ENSP00000217381.2:p.Tyr168LeufsTer2
NM_003098.2:c.503del , LRG_332t1:c.503del NP_003089.1:p.Tyr168LeufsTer2
XM_005260517.1:c.503del XP_005260574.1:p.Tyr168LeufsTer2
XM_011529007.1:c.503del XP_011527309.1:p.Tyr168LeufsTer2
XM_011529008.1:c.503del XP_011527310.1:p.Tyr168LeufsTer2
XR_936612.1:n.736del
XM_024451971.1:c.176del XP_024307739.1:p.Tyr59LeufsTer2
NM_003098.3:c.503del MANE Select NP_003089.1:p.Tyr168LeufsTer2