Canonical Allele Identifier: CA1695091398
Gene: GSDME HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.24698620A= , CM000669.2:g.24698620A= GRCh38
NC_000007.13:g.24738239A= , CM000669.1:g.24738239A= GRCh37
NC_000007.12:g.24704764A= NCBI36
NG_011593.1:g.64401T=

Transcript Alleles

HGVS Amino-acid change
ENST00000342947.9:c.*406T= ENSP00000339587.3:n.*406T=
ENST00000409970.6:c.*406T= ENSP00000387119.1:n.*406T=
ENST00000419307.6:c.*406T= ENSP00000401332.1:n.*406T=
ENST00000645220.1:c.*406T= MANE Select ENSP00000494186.1:n.*406T=
ENST00000342947.7:c.*406T= ENSP00000339587.3:n.*406T=
ENST00000409970.5:c.*406T= ENSP00000387119.1:n.*406T=
ENST00000419307.5:c.*406T= ENSP00000401332.1:n.*406T=
ENST00000479636.1:n.3918T=
NM_001127453.1:c.*406T= NP_001120925.1:n.*406T=
NM_001127454.1:c.*406T= NP_001120926.1:n.*406T=
NM_004403.2:c.*406T= NP_004394.1:n.*406T=
XM_017011802.1:c.*406T= XP_016867291.1:n.*406T=
XM_024446670.1:c.*406T= XP_024302438.1:n.*406T=
NM_004403.3:c.*406T= NP_004394.1:n.*406T=
NM_001127453.2:c.*406T= MANE Select NP_001120925.1:n.*406T=
NM_001127454.2:c.*406T= NP_001120926.1:n.*406T=