Canonical Allele Identifier: CA2259304868
Gene: GSDMB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39906113T= , CM000679.2:g.39906113T= GRCh38
NC_000017.10:g.38062366T= , CM000679.1:g.38062366T= GRCh37
NC_000017.9:g.35315892T= NCBI36
NG_015804.1:g.17538A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000418519.6:c.886A= MANE Select ENSP00000415049.1:p.Arg296=
ENST00000309481.11:c.847A= ENSP00000312584.7:p.Arg283=
ENST00000360317.7:c.886A= ENSP00000353465.3:p.Arg296=
ENST00000394175.6:c.820A= ENSP00000377729.2:p.Arg274=
ENST00000394179.5:c.847A= ENSP00000377733.2:p.Arg283=
ENST00000418519.5:c.886A= ENSP00000415049.1:p.Arg296=
ENST00000468820.1:c.346A=
ENST00000477054.6:n.4074A=
ENST00000479136.5:n.1627A=
ENST00000520542.5:c.859A= ENSP00000430157.1:p.Arg287=
ENST00000522564.5:c.593A= ENSP00000428217.1:n.593A=
ENST00000523371.5:c.762A= ENSP00000429265.1:n.762A=
ENST00000524039.5:c.735A= ENSP00000428712.1:n.735A=
NM_001042471.1:c.847A= NP_001035936.1:p.Arg283=
NM_001165958.1:c.886A= NP_001159430.1:p.Arg296=
NM_001165959.1:c.859A= NP_001159431.1:p.Arg287=
NM_018530.2:c.820A= NP_061000.2:p.Arg274=
XM_011525001.1:c.898A= XP_011523303.1:p.Arg300=
XM_011525002.1:c.898A= XP_011523304.1:p.Arg300=
XM_011525003.1:c.898A= XP_011523305.1:p.Arg300=
XM_011525004.1:c.898A= XP_011523306.1:p.Arg300=
XM_011525005.1:c.898A= XP_011523307.1:p.Arg300=
XM_011525006.1:c.898A= XP_011523308.1:p.Arg300=
XM_011525007.1:c.898A= XP_011523309.1:p.Arg300=
XM_011525008.1:c.898A= XP_011523310.1:p.Arg300=
XM_011525009.1:c.898A= XP_011523311.1:p.Arg300=
XM_011525010.1:c.898A= XP_011523312.1:p.Arg300=
XM_011525011.1:c.898A= XP_011523313.1:p.Arg300=
XM_011525012.1:c.898A= XP_011523314.1:p.Arg300=
XM_011525013.1:c.898A= XP_011523315.1:p.Arg300=
XM_011525014.1:c.898A= XP_011523316.1:p.Arg300=
XM_011525015.1:c.898A= XP_011523317.1:p.Arg300=
XM_011525016.1:c.886A= XP_011523318.1:p.Arg296=
XM_011525017.1:c.871A= XP_011523319.1:p.Arg291=
XM_011525018.1:c.859A= XP_011523320.1:p.Arg287=
XM_011525019.1:c.847A= XP_011523321.1:p.Arg283=
XM_011525020.1:c.820A= XP_011523322.1:p.Arg274=
XR_934504.1:n.2459A=
NM_001369402.1:c.847A= NP_001356331.1:p.Arg283=
NM_001042471.2:c.847A= NP_001035936.1:p.Arg283=
NM_001165958.2:c.886A= MANE Select NP_001159430.1:p.Arg296=
NM_001165959.2:c.859A= NP_001159431.1:p.Arg287=
NM_001369402.2:c.847A= NP_001356331.1:p.Arg283=
NM_001388420.1:c.886A= NP_001375349.1:p.Arg296=
NM_001388421.1:c.859A= NP_001375350.1:p.Arg287=
NM_001388422.1:c.847A= NP_001375351.1:p.Arg283=
NM_001388423.1:c.820A= NP_001375352.1:p.Arg274=
NM_001388424.1:c.577-128A= NP_001375353.1:n.577-128A=
NM_018530.3:c.820A= NP_061000.2:p.Arg274=
NR_170970.1:n.980A=
NR_170971.1:n.2081A=
NR_170972.1:n.1997A=
NR_170973.1:n.2192A=
NR_170974.1:n.2054A=