Canonical Allele Identifier: CA2652478399
Gene: SNTA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33443525_33443526del , CM000682.2:g.33443525_33443526del GRCh38
NC_000020.10:g.32031331_32031332del , CM000682.1:g.32031331_32031332del GRCh37
NC_000020.9:g.31494992_31494993del NCBI36
NG_011622.1:g.5367_5368del , LRG_332:g.5367_5368del

Transcript Alleles

HGVS Amino-acid Change
ENST00000217381.3:c.95_96del MANE Select ENSP00000217381.2:p.Leu32ProfsTer?
ENST00000217381.2:c.95_96del ENSP00000217381.2:p.Leu32ProfsTer?
NM_003098.2:c.95_96del , LRG_332t1:c.95_96del NP_003089.1:p.Leu32ProfsTer?
XM_005260517.1:c.95_96del XP_005260574.1:p.Leu32ProfsTer?
XM_011529007.1:c.95_96del XP_011527309.1:p.Leu32ProfsTer?
XM_011529008.1:c.95_96del XP_011527310.1:p.Leu32ProfsTer?
XR_936612.1:n.328_329del
NM_003098.3:c.95_96del MANE Select NP_003089.1:p.Leu32ProfsTer?