Canonical Allele Identifier: CA1695091388

Gene: GSDME

Linked Data

• dbSNP Id: rs1788731756

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24698619G>A , CM000669.2:g.24698619G>A	GRCh38
NC_000007.13:g.24738238G>A , CM000669.1:g.24738238G>A	GRCh37
NC_000007.12:g.24704763G>A	NCBI36
NG_011593.1:g.64402C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000342947.9:c.*407C>T	ENSP00000339587.3:n.*407C>T
ENST00000409970.6:c.*407C>T	ENSP00000387119.1:n.*407C>T
ENST00000419307.6:c.*407C>T	ENSP00000401332.1:n.*407C>T
ENST00000645220.1:c.*407C>T MANE Select	ENSP00000494186.1:n.*407C>T
ENST00000342947.7:c.*407C>T	ENSP00000339587.3:n.*407C>T
ENST00000409970.5:c.*407C>T	ENSP00000387119.1:n.*407C>T
ENST00000419307.5:c.*407C>T	ENSP00000401332.1:n.*407C>T
ENST00000479636.1:n.3919C>T
NM_001127453.1:c.*407C>T	NP_001120925.1:n.*407C>T
NM_001127454.1:c.*407C>T	NP_001120926.1:n.*407C>T
NM_004403.2:c.*407C>T	NP_004394.1:n.*407C>T
XM_017011802.1:c.*407C>T	XP_016867291.1:n.*407C>T
XM_024446670.1:c.*407C>T	XP_024302438.1:n.*407C>T
NM_004403.3:c.*407C>T	NP_004394.1:n.*407C>T
NM_001127453.2:c.*407C>T MANE Select	NP_001120925.1:n.*407C>T
NM_001127454.2:c.*407C>T	NP_001120926.1:n.*407C>T