Canonical Allele Identifier: CA2504583619

Gene: GSDME

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24698615_24698616insCCCT , CM000669.2:g.24698615_24698616insCCCT	GRCh38
NC_000007.13:g.24738234_24738235insCCCT , CM000669.1:g.24738234_24738235insCCCT	GRCh37
NC_000007.12:g.24704759_24704760insCCCT	NCBI36
NG_011593.1:g.64406_64407insGGGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342947.9:c.*411_*412insGGGA	ENSP00000339587.3:n.*411_*412insGGGA
ENST00000409970.6:c.*411_*412insGGGA	ENSP00000387119.1:n.*411_*412insGGGA
ENST00000419307.6:c.*411_*412insGGGA	ENSP00000401332.1:n.*411_*412insGGGA
ENST00000645220.1:c.*411_*412insGGGA MANE Select	ENSP00000494186.1:n.*411_*412insGGGA
ENST00000342947.7:c.*411_*412insGGGA	ENSP00000339587.3:n.*411_*412insGGGA
ENST00000409970.5:c.*411_*412insGGGA	ENSP00000387119.1:n.*411_*412insGGGA
ENST00000419307.5:c.*411_*412insGGGA	ENSP00000401332.1:n.*411_*412insGGGA
ENST00000479636.1:n.3923_3924insGGGA
NM_001127453.1:c.*411_*412insGGGA	NP_001120925.1:n.*411_*412insGGGA
NM_001127454.1:c.*411_*412insGGGA	NP_001120926.1:n.*411_*412insGGGA
NM_004403.2:c.*411_*412insGGGA	NP_004394.1:n.*411_*412insGGGA
XM_017011802.1:c.*411_*412insGGGA	XP_016867291.1:n.*411_*412insGGGA
XM_024446670.1:c.*411_*412insGGGA	XP_024302438.1:n.*411_*412insGGGA
NM_004403.3:c.*411_*412insGGGA	NP_004394.1:n.*411_*412insGGGA
NM_001127453.2:c.*411_*412insGGGA MANE Select	NP_001120925.1:n.*411_*412insGGGA
NM_001127454.2:c.*411_*412insGGGA	NP_001120926.1:n.*411_*412insGGGA