Canonical Allele Identifier: CA2577372659
Gene: SNTA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33439041_33439043del , CM000682.2:g.33439041_33439043del GRCh38
NC_000020.10:g.32026847_32026849del , CM000682.1:g.32026847_32026849del GRCh37
NC_000020.9:g.31490508_31490510del NCBI36
NG_011622.1:g.9852_9854del , LRG_332:g.9852_9854del

Transcript Alleles

HGVS Amino-acid Change
ENST00000217381.3:c.311-15_311-13del MANE Select ENSP00000217381.2:n.311-15_311-13del
ENST00000217381.2:c.311-15_311-13del ENSP00000217381.2:n.311-15_311-13del
NM_003098.2:c.311-15_311-13del , LRG_332t1:c.311-15_311-13del NP_003089.1:n.311-15_311-13del
XM_005260517.1:c.311-15_311-13del XP_005260574.1:n.311-15_311-13del
XM_011529007.1:c.311-15_311-13del XP_011527309.1:n.311-15_311-13del
XM_011529008.1:c.311-15_311-13del XP_011527310.1:n.311-15_311-13del
XR_936612.1:n.544-15_544-13del
XM_024451971.1:c.-17-15_-17-13del XP_024307739.1:n.-17-15_-17-13del
NM_003098.3:c.311-15_311-13del MANE Select NP_003089.1:n.311-15_311-13del