Canonical Allele Identifier: CA2259304791
Gene: GSDMB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39905930A= , CM000679.2:g.39905930A= GRCh38
NC_000017.10:g.38062183A= , CM000679.1:g.38062183A= GRCh37
NC_000017.9:g.35315709A= NCBI36
NG_015804.1:g.17721T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000418519.6:c.944T= MANE Select ENSP00000415049.1:p.Leu315=
ENST00000309481.11:c.905T= ENSP00000312584.7:p.Leu302=
ENST00000360317.7:c.944T= ENSP00000353465.3:p.Leu315=
ENST00000394175.6:c.878T= ENSP00000377729.2:p.Leu293=
ENST00000394179.5:c.905T= ENSP00000377733.2:p.Leu302=
ENST00000418519.5:c.944T= ENSP00000415049.1:p.Leu315=
ENST00000477054.6:n.4132T=
ENST00000479136.5:n.1685T=
ENST00000486560.1:n.9T=
ENST00000520542.5:c.917T= ENSP00000430157.1:p.Leu306=
ENST00000522564.5:c.651T= ENSP00000428217.1:n.651T=
ENST00000523371.5:c.820T= ENSP00000429265.1:n.820T=
ENST00000524039.5:c.793T= ENSP00000428712.1:n.793T=
NM_001042471.1:c.905T= NP_001035936.1:p.Leu302=
NM_001165958.1:c.944T= NP_001159430.1:p.Leu315=
NM_001165959.1:c.917T= NP_001159431.1:p.Leu306=
NM_018530.2:c.878T= NP_061000.2:p.Leu293=
XM_011525001.1:c.956T= XP_011523303.1:p.Leu319=
XM_011525002.1:c.956T= XP_011523304.1:p.Leu319=
XM_011525003.1:c.956T= XP_011523305.1:p.Leu319=
XM_011525004.1:c.956T= XP_011523306.1:p.Leu319=
XM_011525005.1:c.956T= XP_011523307.1:p.Leu319=
XM_011525006.1:c.956T= XP_011523308.1:p.Leu319=
XM_011525007.1:c.956T= XP_011523309.1:p.Leu319=
XM_011525008.1:c.956T= XP_011523310.1:p.Leu319=
XM_011525009.1:c.956T= XP_011523311.1:p.Leu319=
XM_011525010.1:c.956T= XP_011523312.1:p.Leu319=
XM_011525011.1:c.956T= XP_011523313.1:p.Leu319=
XM_011525012.1:c.956T= XP_011523314.1:p.Leu319=
XM_011525013.1:c.956T= XP_011523315.1:p.Leu319=
XM_011525014.1:c.956T= XP_011523316.1:p.Leu319=
XM_011525015.1:c.956T= XP_011523317.1:p.Leu319=
XM_011525016.1:c.944T= XP_011523318.1:p.Leu315=
XM_011525017.1:c.929T= XP_011523319.1:p.Leu310=
XM_011525018.1:c.917T= XP_011523320.1:p.Leu306=
XM_011525019.1:c.905T= XP_011523321.1:p.Leu302=
XM_011525020.1:c.878T= XP_011523322.1:p.Leu293=
XR_934504.1:n.2517T=
NM_001369402.1:c.905T= NP_001356331.1:p.Leu302=
NM_001042471.2:c.905T= NP_001035936.1:p.Leu302=
NM_001165958.2:c.944T= MANE Select NP_001159430.1:p.Leu315=
NM_001165959.2:c.917T= NP_001159431.1:p.Leu306=
NM_001369402.2:c.905T= NP_001356331.1:p.Leu302=
NM_001388420.1:c.944T= NP_001375349.1:p.Leu315=
NM_001388421.1:c.917T= NP_001375350.1:p.Leu306=
NM_001388422.1:c.905T= NP_001375351.1:p.Leu302=
NM_001388423.1:c.878T= NP_001375352.1:p.Leu293=
NM_001388424.1:c.632T= NP_001375353.1:p.Leu211=
NM_018530.3:c.878T= NP_061000.2:p.Leu293=
NR_170970.1:n.1038T=
NR_170971.1:n.2139T=
NR_170972.1:n.2055T=
NR_170973.1:n.2250T=
NR_170974.1:n.2112T=