Canonical Allele Identifier: CA1695091364
Gene: GSDME HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.24698607C= , CM000669.2:g.24698607C= GRCh38
NC_000007.13:g.24738226C= , CM000669.1:g.24738226C= GRCh37
NC_000007.12:g.24704751C= NCBI36
NG_011593.1:g.64414G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342947.9:c.*419G= ENSP00000339587.3:n.*419G=
ENST00000409970.6:c.*419G= ENSP00000387119.1:n.*419G=
ENST00000419307.6:c.*419G= ENSP00000401332.1:n.*419G=
ENST00000645220.1:c.*419G= MANE Select ENSP00000494186.1:n.*419G=
ENST00000342947.7:c.*419G= ENSP00000339587.3:n.*419G=
ENST00000409970.5:c.*419G= ENSP00000387119.1:n.*419G=
ENST00000419307.5:c.*419G= ENSP00000401332.1:n.*419G=
ENST00000479636.1:n.3931G=
NM_001127453.1:c.*419G= NP_001120925.1:n.*419G=
NM_001127454.1:c.*419G= NP_001120926.1:n.*419G=
NM_004403.2:c.*419G= NP_004394.1:n.*419G=
XM_017011802.1:c.*419G= XP_016867291.1:n.*419G=
XM_024446670.1:c.*419G= XP_024302438.1:n.*419G=
NM_004403.3:c.*419G= NP_004394.1:n.*419G=
NM_001127453.2:c.*419G= MANE Select NP_001120925.1:n.*419G=
NM_001127454.2:c.*419G= NP_001120926.1:n.*419G=