Canonical Allele Identifier: CA2682082217
Gene: GSDME HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.24717206_24717207insAATCCTCTGCTGGGGGTCCCTCTGCTGAGG , CM000669.2:g.24717206_24717207insAATCCTCTGCTGGGGGTCCCTCTGCTGAGG GRCh38
NC_000007.13:g.24756825_24756826insAATCCTCTGCTGGGGGTCCCTCTGCTGAGG , CM000669.1:g.24756825_24756826insAATCCTCTGCTGGGGGTCCCTCTGCTGAGG GRCh37
NC_000007.12:g.24723350_24723351insAATCCTCTGCTGGGGGTCCCTCTGCTGAGG NCBI36
NG_011593.1:g.45829_45830insCCCCAGCAGAGGATTCCTCAGCAGAGGGAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000342947.9:c.697+62_697+63insCCCCAGCAGAGGATTCCTCAGCAGAGGGAC ENSP00000339587.3:n.697+62_697+63insCCCCAGCAGAGGATTCCTCAGCAGA...
ENST00000409970.6:c.205+62_205+63insCCCCAGCAGAGGATTCCTCAGCAGAGGGAC ENSP00000387119.1:n.205+62_205+63insCCCCAGCAGAGGATTCCTCAGCAGA...
ENST00000411476.3:n.466+62_466+63insCCCCAGCAGAGGATTCCTCAGCAGAGGGAC
ENST00000414428.2:c.697+62_697+63insCCCCAGCAGAGGATTCCTCAGCAGAGGGAC ENSP00000413963.2:n.697+62_697+63insCCCCAGCAGAGGATTCCTCAGCAGA...
ENST00000419307.6:c.205+62_205+63insCCCCAGCAGAGGATTCCTCAGCAGAGGGAC ENSP00000401332.1:n.205+62_205+63insCCCCAGCAGAGGATTCCTCAGCAGA...
ENST00000446822.6:c.171+62_171+63insCCCCAGCAGAGGATTCCTCAGCAGAGGGAC
ENST00000559637.6:n.392+62_392+63insCCCCAGCAGAGGATTCCTCAGCAGAGGGAC
ENST00000645220.1:c.697+62_697+63insCCCCAGCAGAGGATTCCTCAGCAGAGGGAC MANE Select ENSP00000494186.1:n.697+62_697+63insCCCCAGCAGAGGATTCCTCAGCAGA...
ENST00000342947.7:c.697+62_697+63insCCCCAGCAGAGGATTCCTCAGCAGAGGGAC ENSP00000339587.3:n.697+62_697+63insCCCCAGCAGAGGATTCCTCAGCAGA...
ENST00000409775.7:c.697+62_697+63insCCCCAGCAGAGGATTCCTCAGCAGAGGGAC ENSP00000386670.3:n.697+62_697+63insCCCCAGCAGAGGATTCCTCAGCAGA...
ENST00000409970.5:c.205+62_205+63insCCCCAGCAGAGGATTCCTCAGCAGAGGGAC ENSP00000387119.1:n.205+62_205+63insCCCCAGCAGAGGATTCCTCAGCAGA...
ENST00000411476.2:c.466+62_466+63insCCCCAGCAGAGGATTCCTCAGCAGAGGGAC ENSP00000414090.2:n.466+62_466+63insCCCCAGCAGAGGATTCCTCAGCAGA...
ENST00000415480.5:c.63+62_63+63insCCCCAGCAGAGGATTCCTCAGCAGAGGGAC
ENST00000419307.5:c.205+62_205+63insCCCCAGCAGAGGATTCCTCAGCAGAGGGAC ENSP00000401332.1:n.205+62_205+63insCCCCAGCAGAGGATTCCTCAGCAGA...
ENST00000446822.5:c.171+62_171+63insCCCCAGCAGAGGATTCCTCAGCAGAGGGAC
ENST00000493723.5:n.778_779insCCCCAGCAGAGGATTCCTCAGCAGAGGGAC
ENST00000559637.5:n.392+62_392+63insCCCCAGCAGAGGATTCCTCAGCAGAGGGAC
NM_001127453.1:c.697+62_697+63insCCCCAGCAGAGGATTCCTCAGCAGAGGGAC NP_001120925.1:n.697+62_697+63insCCCCAGCAGAGGATTCCTCAGCAGAGGG...
NM_001127454.1:c.205+62_205+63insCCCCAGCAGAGGATTCCTCAGCAGAGGGAC NP_001120926.1:n.205+62_205+63insCCCCAGCAGAGGATTCCTCAGCAGAGGG...
NM_004403.2:c.697+62_697+63insCCCCAGCAGAGGATTCCTCAGCAGAGGGAC NP_004394.1:n.697+62_697+63insCCCCAGCAGAGGATTCCTCAGCAGAGGGAC
XM_017011802.1:c.205+62_205+63insCCCCAGCAGAGGATTCCTCAGCAGAGGGAC XP_016867291.1:n.205+62_205+63insCCCCAGCAGAGGATTCCTCAGCAGAGGG...
XM_024446670.1:c.697+62_697+63insCCCCAGCAGAGGATTCCTCAGCAGAGGGAC XP_024302438.1:n.697+62_697+63insCCCCAGCAGAGGATTCCTCAGCAGAGGG...
NM_004403.3:c.697+62_697+63insCCCCAGCAGAGGATTCCTCAGCAGAGGGAC NP_004394.1:n.697+62_697+63insCCCCAGCAGAGGATTCCTCAGCAGAGGGAC
NM_001127453.2:c.697+62_697+63insCCCCAGCAGAGGATTCCTCAGCAGAGGGAC MANE Select NP_001120925.1:n.697+62_697+63insCCCCAGCAGAGGATTCCTCAGCAGAGGG...
NM_001127454.2:c.205+62_205+63insCCCCAGCAGAGGATTCCTCAGCAGAGGGAC NP_001120926.1:n.205+62_205+63insCCCCAGCAGAGGATTCCTCAGCAGAGGG...