Canonical Allele Identifier: CA2259304873
Gene: GSDMB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39906129C= , CM000679.2:g.39906129C= GRCh38
NC_000017.10:g.38062382C= , CM000679.1:g.38062382C= GRCh37
NC_000017.9:g.35315908C= NCBI36
NG_015804.1:g.17522G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000418519.6:c.870G= MANE Select ENSP00000415049.1:p.Arg290=
ENST00000309481.11:c.831G= ENSP00000312584.7:p.Arg277=
ENST00000360317.7:c.870G= ENSP00000353465.3:p.Arg290=
ENST00000394175.6:c.804G= ENSP00000377729.2:p.Arg268=
ENST00000394179.5:c.831G= ENSP00000377733.2:p.Arg277=
ENST00000418519.5:c.870G= ENSP00000415049.1:p.Arg290=
ENST00000468820.1:c.330G=
ENST00000477054.6:n.4058G=
ENST00000479136.5:n.1611G=
ENST00000520542.5:c.843G= ENSP00000430157.1:p.Arg281=
ENST00000522564.5:c.577G= ENSP00000428217.1:n.577G=
ENST00000523371.5:c.746G= ENSP00000429265.1:n.746G=
ENST00000524039.5:c.719G= ENSP00000428712.1:n.719G=
NM_001042471.1:c.831G= NP_001035936.1:p.Arg277=
NM_001165958.1:c.870G= NP_001159430.1:p.Arg290=
NM_001165959.1:c.843G= NP_001159431.1:p.Arg281=
NM_018530.2:c.804G= NP_061000.2:p.Arg268=
XM_011525001.1:c.882G= XP_011523303.1:p.Arg294=
XM_011525002.1:c.882G= XP_011523304.1:p.Arg294=
XM_011525003.1:c.882G= XP_011523305.1:p.Arg294=
XM_011525004.1:c.882G= XP_011523306.1:p.Arg294=
XM_011525005.1:c.882G= XP_011523307.1:p.Arg294=
XM_011525006.1:c.882G= XP_011523308.1:p.Arg294=
XM_011525007.1:c.882G= XP_011523309.1:p.Arg294=
XM_011525008.1:c.882G= XP_011523310.1:p.Arg294=
XM_011525009.1:c.882G= XP_011523311.1:p.Arg294=
XM_011525010.1:c.882G= XP_011523312.1:p.Arg294=
XM_011525011.1:c.882G= XP_011523313.1:p.Arg294=
XM_011525012.1:c.882G= XP_011523314.1:p.Arg294=
XM_011525013.1:c.882G= XP_011523315.1:p.Arg294=
XM_011525014.1:c.882G= XP_011523316.1:p.Arg294=
XM_011525015.1:c.882G= XP_011523317.1:p.Arg294=
XM_011525016.1:c.870G= XP_011523318.1:p.Arg290=
XM_011525017.1:c.855G= XP_011523319.1:p.Arg285=
XM_011525018.1:c.843G= XP_011523320.1:p.Arg281=
XM_011525019.1:c.831G= XP_011523321.1:p.Arg277=
XM_011525020.1:c.804G= XP_011523322.1:p.Arg268=
XR_934504.1:n.2443G=
NM_001369402.1:c.831G= NP_001356331.1:p.Arg277=
NM_001042471.2:c.831G= NP_001035936.1:p.Arg277=
NM_001165958.2:c.870G= MANE Select NP_001159430.1:p.Arg290=
NM_001165959.2:c.843G= NP_001159431.1:p.Arg281=
NM_001369402.2:c.831G= NP_001356331.1:p.Arg277=
NM_001388420.1:c.870G= NP_001375349.1:p.Arg290=
NM_001388421.1:c.843G= NP_001375350.1:p.Arg281=
NM_001388422.1:c.831G= NP_001375351.1:p.Arg277=
NM_001388423.1:c.804G= NP_001375352.1:p.Arg268=
NM_001388424.1:c.577-144G= NP_001375353.1:n.577-144G=
NM_018530.3:c.804G= NP_061000.2:p.Arg268=
NR_170970.1:n.964G=
NR_170971.1:n.2065G=
NR_170972.1:n.1981G=
NR_170973.1:n.2176G=
NR_170974.1:n.2038G=