Canonical Allele Identifier: CA1695071627
Gene: GSDME HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.24719102A= , CM000669.2:g.24719102A= GRCh38
NC_000007.13:g.24758721A= , CM000669.1:g.24758721A= GRCh37
NC_000007.12:g.24725246A= NCBI36
NG_011593.1:g.43919T=

Transcript Alleles

HGVS Amino-acid change
ENST00000342947.9:c.521T= ENSP00000339587.3:p.Met174=
ENST00000409970.6:c.29T= ENSP00000387119.1:p.Met10=
ENST00000411476.3:n.290T=
ENST00000414428.2:c.521T= ENSP00000413963.2:p.Met174=
ENST00000419307.6:c.29T= ENSP00000401332.1:p.Met10=
ENST00000559637.6:n.216T=
ENST00000645220.1:c.521T= MANE Select ENSP00000494186.1:p.Met174=
ENST00000342947.7:c.521T= ENSP00000339587.3:p.Met174=
ENST00000409775.7:c.521T= ENSP00000386670.3:p.Met174=
ENST00000409970.5:c.29T= ENSP00000387119.1:p.Met10=
ENST00000411476.2:c.290T= ENSP00000414090.2:p.Met97=
ENST00000414428.1:c.29T= ENSP00000413963.1:p.Met10=
ENST00000419307.5:c.29T= ENSP00000401332.1:p.Met10=
ENST00000493723.5:n.540T=
ENST00000559637.5:n.216T=
NM_001127453.1:c.521T= NP_001120925.1:p.Met174=
NM_001127454.1:c.29T= NP_001120926.1:p.Met10=
NM_004403.2:c.521T= NP_004394.1:p.Met174=
XM_017011802.1:c.29T= XP_016867291.1:p.Met10=
XM_024446670.1:c.521T= XP_024302438.1:p.Met174=
NM_004403.3:c.521T= NP_004394.1:p.Met174=
NM_001127453.2:c.521T= MANE Select NP_001120925.1:p.Met174=
NM_001127454.2:c.29T= NP_001120926.1:p.Met10=