Canonical Allele Identifier: CA273667
Gene: GSDME HGNC NCBI

Linked Data

dbSNP Id: rs727505273

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.24706396_24706398del , CM000669.2:g.24706396_24706398del GRCh38
NC_000007.13:g.24746015_24746017del , CM000669.1:g.24746015_24746017del GRCh37
NC_000007.12:g.24712540_24712542del NCBI36
NG_011593.1:g.56630_56632del

Transcript Alleles

HGVS Amino-acid change
ENST00000342947.9:c.991-15_991-13del ENSP00000339587.3:n.991-15_991-13del
ENST00000409970.6:c.499-15_499-13del ENSP00000387119.1:n.499-15_499-13del
ENST00000419307.6:c.499-15_499-13del ENSP00000401332.1:n.499-15_499-13del
ENST00000645220.1:c.991-15_991-13del MANE Select ENSP00000494186.1:n.991-15_991-13del
ENST00000342947.7:c.991-15_991-13del ENSP00000339587.3:n.991-15_991-13del
ENST00000409775.7:c.991-15_991-13del ENSP00000386670.3:n.991-15_991-13del
ENST00000409970.5:c.499-15_499-13del ENSP00000387119.1:n.499-15_499-13del
ENST00000419307.5:c.499-15_499-13del ENSP00000401332.1:n.499-15_499-13del
NM_001127453.1:c.991-15_991-13del NP_001120925.1:n.991-15_991-13del
NM_001127454.1:c.499-15_499-13del NP_001120926.1:n.499-15_499-13del
NM_004403.2:c.991-15_991-13del NP_004394.1:n.991-15_991-13del
XM_017011802.1:c.499-15_499-13del XP_016867291.1:n.499-15_499-13del
XM_024446670.1:c.991-15_991-13del XP_024302438.1:n.991-15_991-13del
NM_004403.3:c.991-15_991-13del NP_004394.1:n.991-15_991-13del
NM_001127453.2:c.991-15_991-13del MANE Select NP_001120925.1:n.991-15_991-13del
NM_001127454.2:c.499-15_499-13del NP_001120926.1:n.499-15_499-13del