Canonical Allele Identifier: CA1099433647

Gene: GSDME

Linked Data

• gnomAD v3: 7-24717191-A-AGTCCCTCTGCTTAGGTATCCTCTGCTGGGG
• gnomAD v4: 7-24717191-A-AGTCCCTCTGCTTAGGTATCCTCTGCTGGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24717202_24717203insTAGGTATCCTCTGCTGGGGGTCCCTCTGCT , CM000669.2:g.24717202_24717203insTAGGTATCCTCTGCTGGGGGTCCCTCTGCT	GRCh38
NC_000007.13:g.24756821_24756822insTAGGTATCCTCTGCTGGGGGTCCCTCTGCT , CM000669.1:g.24756821_24756822insTAGGTATCCTCTGCTGGGGGTCCCTCTGCT	GRCh37
NC_000007.12:g.24723346_24723347insTAGGTATCCTCTGCTGGGGGTCCCTCTGCT	NCBI36
NG_011593.1:g.45829_45830insCCCCAGCAGAGGATACCTAAGCAGAGGGAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342947.9:c.697+62_697+63insCCCCAGCAGAGGATACCTAAGCAGAGGGAC	ENSP00000339587.3:n.697+62_697+63insCCCCAGCAGAGGATACCTAAGCAGA...
ENST00000409970.6:c.205+62_205+63insCCCCAGCAGAGGATACCTAAGCAGAGGGAC	ENSP00000387119.1:n.205+62_205+63insCCCCAGCAGAGGATACCTAAGCAGA...
ENST00000411476.3:n.466+62_466+63insCCCCAGCAGAGGATACCTAAGCAGAGGGAC
ENST00000414428.2:c.697+62_697+63insCCCCAGCAGAGGATACCTAAGCAGAGGGAC	ENSP00000413963.2:n.697+62_697+63insCCCCAGCAGAGGATACCTAAGCAGA...
ENST00000419307.6:c.205+62_205+63insCCCCAGCAGAGGATACCTAAGCAGAGGGAC	ENSP00000401332.1:n.205+62_205+63insCCCCAGCAGAGGATACCTAAGCAGA...
ENST00000446822.6:c.171+62_171+63insCCCCAGCAGAGGATACCTAAGCAGAGGGAC
ENST00000559637.6:n.392+62_392+63insCCCCAGCAGAGGATACCTAAGCAGAGGGAC
ENST00000645220.1:c.697+62_697+63insCCCCAGCAGAGGATACCTAAGCAGAGGGAC MANE Select	ENSP00000494186.1:n.697+62_697+63insCCCCAGCAGAGGATACCTAAGCAGA...
ENST00000342947.7:c.697+62_697+63insCCCCAGCAGAGGATACCTAAGCAGAGGGAC	ENSP00000339587.3:n.697+62_697+63insCCCCAGCAGAGGATACCTAAGCAGA...
ENST00000409775.7:c.697+62_697+63insCCCCAGCAGAGGATACCTAAGCAGAGGGAC	ENSP00000386670.3:n.697+62_697+63insCCCCAGCAGAGGATACCTAAGCAGA...
ENST00000409970.5:c.205+62_205+63insCCCCAGCAGAGGATACCTAAGCAGAGGGAC	ENSP00000387119.1:n.205+62_205+63insCCCCAGCAGAGGATACCTAAGCAGA...
ENST00000411476.2:c.466+62_466+63insCCCCAGCAGAGGATACCTAAGCAGAGGGAC	ENSP00000414090.2:n.466+62_466+63insCCCCAGCAGAGGATACCTAAGCAGA...
ENST00000415480.5:c.63+62_63+63insCCCCAGCAGAGGATACCTAAGCAGAGGGAC
ENST00000419307.5:c.205+62_205+63insCCCCAGCAGAGGATACCTAAGCAGAGGGAC	ENSP00000401332.1:n.205+62_205+63insCCCCAGCAGAGGATACCTAAGCAGA...
ENST00000446822.5:c.171+62_171+63insCCCCAGCAGAGGATACCTAAGCAGAGGGAC
ENST00000493723.5:n.778_779insCCCCAGCAGAGGATACCTAAGCAGAGGGAC
ENST00000559637.5:n.392+62_392+63insCCCCAGCAGAGGATACCTAAGCAGAGGGAC
NM_001127453.1:c.697+62_697+63insCCCCAGCAGAGGATACCTAAGCAGAGGGAC	NP_001120925.1:n.697+62_697+63insCCCCAGCAGAGGATACCTAAGCAGAGGG...
NM_001127454.1:c.205+62_205+63insCCCCAGCAGAGGATACCTAAGCAGAGGGAC	NP_001120926.1:n.205+62_205+63insCCCCAGCAGAGGATACCTAAGCAGAGGG...
NM_004403.2:c.697+62_697+63insCCCCAGCAGAGGATACCTAAGCAGAGGGAC	NP_004394.1:n.697+62_697+63insCCCCAGCAGAGGATACCTAAGCAGAGGGAC
XM_017011802.1:c.205+62_205+63insCCCCAGCAGAGGATACCTAAGCAGAGGGAC	XP_016867291.1:n.205+62_205+63insCCCCAGCAGAGGATACCTAAGCAGAGGG...
XM_024446670.1:c.697+62_697+63insCCCCAGCAGAGGATACCTAAGCAGAGGGAC	XP_024302438.1:n.697+62_697+63insCCCCAGCAGAGGATACCTAAGCAGAGGG...
NM_004403.3:c.697+62_697+63insCCCCAGCAGAGGATACCTAAGCAGAGGGAC	NP_004394.1:n.697+62_697+63insCCCCAGCAGAGGATACCTAAGCAGAGGGAC
NM_001127453.2:c.697+62_697+63insCCCCAGCAGAGGATACCTAAGCAGAGGGAC MANE Select	NP_001120925.1:n.697+62_697+63insCCCCAGCAGAGGATACCTAAGCAGAGGG...
NM_001127454.2:c.205+62_205+63insCCCCAGCAGAGGATACCTAAGCAGAGGGAC	NP_001120926.1:n.205+62_205+63insCCCCAGCAGAGGATACCTAAGCAGAGGG...