Canonical Allele Identifier: CA2637651542

Gene: GSDMB

Linked Data

• gnomAD v4: 17-39906071-CTA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39906073_39906074del , CM000679.2:g.39906073_39906074del	GRCh38
NC_000017.10:g.38062326_38062327del , CM000679.1:g.38062326_38062327del	GRCh37
NC_000017.9:g.35315852_35315853del	NCBI36
NG_015804.1:g.17578_17579del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000418519.6:c.888+38_888+39del MANE Select	ENSP00000415049.1:n.888+38_888+39del
ENST00000309481.11:c.849+38_849+39del	ENSP00000312584.7:n.849+38_849+39del
ENST00000360317.7:c.888+38_888+39del	ENSP00000353465.3:n.888+38_888+39del
ENST00000394175.6:c.822+38_822+39del	ENSP00000377729.2:n.822+38_822+39del
ENST00000394179.5:c.849+38_849+39del	ENSP00000377733.2:n.849+38_849+39del
ENST00000418519.5:c.888+38_888+39del	ENSP00000415049.1:n.888+38_888+39del
ENST00000468820.1:c.348+38_348+39del
ENST00000477054.6:n.4076+38_4076+39del
ENST00000479136.5:n.1629+38_1629+39del
ENST00000520542.5:c.861+38_861+39del	ENSP00000430157.1:n.861+38_861+39del
ENST00000522564.5:c.595+38_595+39del	ENSP00000428217.1:n.595+38_595+39del
ENST00000523371.5:c.764+38_764+39del	ENSP00000429265.1:n.764+38_764+39del
ENST00000524039.5:c.737+38_737+39del	ENSP00000428712.1:n.737+38_737+39del
NM_001042471.1:c.849+38_849+39del	NP_001035936.1:n.849+38_849+39del
NM_001165958.1:c.888+38_888+39del	NP_001159430.1:n.888+38_888+39del
NM_001165959.1:c.861+38_861+39del	NP_001159431.1:n.861+38_861+39del
NM_018530.2:c.822+38_822+39del	NP_061000.2:n.822+38_822+39del
XM_011525001.1:c.900+38_900+39del	XP_011523303.1:n.900+38_900+39del
XM_011525002.1:c.900+38_900+39del	XP_011523304.1:n.900+38_900+39del
XM_011525003.1:c.900+38_900+39del	XP_011523305.1:n.900+38_900+39del
XM_011525004.1:c.900+38_900+39del	XP_011523306.1:n.900+38_900+39del
XM_011525005.1:c.900+38_900+39del	XP_011523307.1:n.900+38_900+39del
XM_011525006.1:c.900+38_900+39del	XP_011523308.1:n.900+38_900+39del
XM_011525007.1:c.900+38_900+39del	XP_011523309.1:n.900+38_900+39del
XM_011525008.1:c.900+38_900+39del	XP_011523310.1:n.900+38_900+39del
XM_011525009.1:c.900+38_900+39del	XP_011523311.1:n.900+38_900+39del
XM_011525010.1:c.900+38_900+39del	XP_011523312.1:n.900+38_900+39del
XM_011525011.1:c.900+38_900+39del	XP_011523313.1:n.900+38_900+39del
XM_011525012.1:c.900+38_900+39del	XP_011523314.1:n.900+38_900+39del
XM_011525013.1:c.900+38_900+39del	XP_011523315.1:n.900+38_900+39del
XM_011525014.1:c.900+38_900+39del	XP_011523316.1:n.900+38_900+39del
XM_011525015.1:c.900+38_900+39del	XP_011523317.1:n.900+38_900+39del
XM_011525016.1:c.888+38_888+39del	XP_011523318.1:n.888+38_888+39del
XM_011525017.1:c.873+38_873+39del	XP_011523319.1:n.873+38_873+39del
XM_011525018.1:c.861+38_861+39del	XP_011523320.1:n.861+38_861+39del
XM_011525019.1:c.849+38_849+39del	XP_011523321.1:n.849+38_849+39del
XM_011525020.1:c.822+38_822+39del	XP_011523322.1:n.822+38_822+39del
XR_934504.1:n.2461+38_2461+39del
NM_001369402.1:c.849+38_849+39del	NP_001356331.1:n.849+38_849+39del
NM_001042471.2:c.849+38_849+39del	NP_001035936.1:n.849+38_849+39del
NM_001165958.2:c.888+38_888+39del MANE Select	NP_001159430.1:n.888+38_888+39del
NM_001165959.2:c.861+38_861+39del	NP_001159431.1:n.861+38_861+39del
NM_001369402.2:c.849+38_849+39del	NP_001356331.1:n.849+38_849+39del
NM_001388420.1:c.888+38_888+39del	NP_001375349.1:n.888+38_888+39del
NM_001388421.1:c.861+38_861+39del	NP_001375350.1:n.861+38_861+39del
NM_001388422.1:c.849+38_849+39del	NP_001375351.1:n.849+38_849+39del
NM_001388423.1:c.822+38_822+39del	NP_001375352.1:n.822+38_822+39del
NM_001388424.1:c.577-88_577-87del	NP_001375353.1:n.577-88_577-87del
NM_018530.3:c.822+38_822+39del	NP_061000.2:n.822+38_822+39del
NR_170970.1:n.982+38_982+39del
NR_170971.1:n.2083+38_2083+39del
NR_170972.1:n.1999+38_1999+39del
NR_170973.1:n.2194+38_2194+39del
NR_170974.1:n.2056+38_2056+39del