Canonical Allele Identifier: CA836952335

Gene: GSDME

Linked Data

• dbSNP Id: rs1167836610
• gnomAD v3: 7-24698417-C-T
• gnomAD v4: 7-24698417-C-T
• MyVariant Identifiers: chr7:g.24738036C>T (hg19) ; chr7:g.24698417C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24698417C>T , CM000669.2:g.24698417C>T	GRCh38
NC_000007.13:g.24738036C>T , CM000669.1:g.24738036C>T	GRCh37
NC_000007.12:g.24704561C>T	NCBI36
NG_011593.1:g.64604G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342947.9:c.*609G>A	ENSP00000339587.3:n.*609G>A
ENST00000409970.6:c.*609G>A	ENSP00000387119.1:n.*609G>A
ENST00000645220.1:c.*609G>A MANE Select	ENSP00000494186.1:n.*609G>A
ENST00000342947.7:c.*609G>A	ENSP00000339587.3:n.*609G>A
ENST00000409970.5:c.*609G>A	ENSP00000387119.1:n.*609G>A
ENST00000419307.5:c.*609G>A	ENSP00000401332.1:n.*609G>A
ENST00000479636.1:n.4121G>A
NM_001127453.1:c.*609G>A	NP_001120925.1:n.*609G>A
NM_001127454.1:c.*609G>A	NP_001120926.1:n.*609G>A
NM_004403.2:c.*609G>A	NP_004394.1:n.*609G>A
XM_017011802.1:c.*609G>A	XP_016867291.1:n.*609G>A
XM_024446670.1:c.*609G>A	XP_024302438.1:n.*609G>A
NM_004403.3:c.*609G>A	NP_004394.1:n.*609G>A
NM_001127453.2:c.*609G>A MANE Select	NP_001120925.1:n.*609G>A
NM_001127454.2:c.*609G>A	NP_001120926.1:n.*609G>A