Canonical Allele Identifier: CA2577372660
Gene: SNTA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33439056del , CM000682.2:g.33439056del GRCh38
NC_000020.10:g.32026862del , CM000682.1:g.32026862del GRCh37
NC_000020.9:g.31490523del NCBI36
NG_011622.1:g.9838del , LRG_332:g.9838del

Transcript Alleles

HGVS Amino-acid Change
ENST00000217381.3:c.311-29del MANE Select ENSP00000217381.2:n.311-29del
ENST00000217381.2:c.311-29del ENSP00000217381.2:n.311-29del
NM_003098.2:c.311-29del , LRG_332t1:c.311-29del NP_003089.1:n.311-29del
XM_005260517.1:c.311-29del XP_005260574.1:n.311-29del
XM_011529007.1:c.311-29del XP_011527309.1:n.311-29del
XM_011529008.1:c.311-29del XP_011527310.1:n.311-29del
XR_936612.1:n.544-29del
XM_024451971.1:c.-17-29del XP_024307739.1:n.-17-29del
NM_003098.3:c.311-29del MANE Select NP_003089.1:n.311-29del