Canonical Allele Identifier: CA1695091443
Gene: GSDME HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.24698669A= , CM000669.2:g.24698669A= GRCh38
NC_000007.13:g.24738288A= , CM000669.1:g.24738288A= GRCh37
NC_000007.12:g.24704813A= NCBI36
NG_011593.1:g.64352T=

Transcript Alleles

HGVS Amino-acid change
ENST00000342947.9:c.*357T= ENSP00000339587.3:n.*357T=
ENST00000409970.6:c.*357T= ENSP00000387119.1:n.*357T=
ENST00000419307.6:c.*357T= ENSP00000401332.1:n.*357T=
ENST00000645220.1:c.*357T= MANE Select ENSP00000494186.1:n.*357T=
ENST00000342947.7:c.*357T= ENSP00000339587.3:n.*357T=
ENST00000409970.5:c.*357T= ENSP00000387119.1:n.*357T=
ENST00000419307.5:c.*357T= ENSP00000401332.1:n.*357T=
ENST00000479636.1:n.3869T=
NM_001127453.1:c.*357T= NP_001120925.1:n.*357T=
NM_001127454.1:c.*357T= NP_001120926.1:n.*357T=
NM_004403.2:c.*357T= NP_004394.1:n.*357T=
XM_017011802.1:c.*357T= XP_016867291.1:n.*357T=
XM_024446670.1:c.*357T= XP_024302438.1:n.*357T=
NM_004403.3:c.*357T= NP_004394.1:n.*357T=
NM_001127453.2:c.*357T= MANE Select NP_001120925.1:n.*357T=
NM_001127454.2:c.*357T= NP_001120926.1:n.*357T=