Canonical Allele Identifier: CA367047950

Gene: GSDME

Linked Data

• MyVariant Identifiers: chr7:g.24756912C>G (hg19) ; chr7:g.24717293C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24717293C>G , CM000669.2:g.24717293C>G	GRCh38
NC_000007.13:g.24756912C>G , CM000669.1:g.24756912C>G	GRCh37
NC_000007.12:g.24723437C>G	NCBI36
NG_011593.1:g.45728G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342947.9:c.658G>C	ENSP00000339587.3:p.Gly220Arg
ENST00000409970.6:c.166G>C	ENSP00000387119.1:p.Gly56Arg
ENST00000411476.3:n.427G>C
ENST00000414428.2:c.658G>C	ENSP00000413963.2:p.Gly220Arg
ENST00000419307.6:c.166G>C	ENSP00000401332.1:p.Gly56Arg
ENST00000446822.6:c.132G>C
ENST00000559637.6:n.353G>C
ENST00000645220.1:c.658G>C MANE Select	ENSP00000494186.1:p.Gly220Arg
ENST00000342947.7:c.658G>C	ENSP00000339587.3:p.Gly220Arg
ENST00000409775.7:c.658G>C	ENSP00000386670.3:p.Gly220Arg
ENST00000409970.5:c.166G>C	ENSP00000387119.1:p.Gly56Arg
ENST00000411476.2:c.427G>C	ENSP00000414090.2:p.Gly143Arg
ENST00000415480.5:c.24G>C
ENST00000419307.5:c.166G>C	ENSP00000401332.1:p.Gly56Arg
ENST00000446822.5:c.132G>C
ENST00000493723.5:n.677G>C
ENST00000559637.5:n.353G>C
NM_001127453.1:c.658G>C	NP_001120925.1:p.Gly220Arg
NM_001127454.1:c.166G>C	NP_001120926.1:p.Gly56Arg
NM_004403.2:c.658G>C	NP_004394.1:p.Gly220Arg
XM_017011802.1:c.166G>C	XP_016867291.1:p.Gly56Arg
XM_024446670.1:c.658G>C	XP_024302438.1:p.Gly220Arg
NM_004403.3:c.658G>C	NP_004394.1:p.Gly220Arg
NM_001127453.2:c.658G>C MANE Select	NP_001120925.1:p.Gly220Arg
NM_001127454.2:c.166G>C	NP_001120926.1:p.Gly56Arg