Canonical Allele Identifier: CA2561957442

Gene: HMBS

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119085177_119085178insCTTTTTTTTTTTTTTTT , CM000673.2:g.119085177_119085178insCTTTTTTTTTTTTTTTT	GRCh38
NC_000011.9:g.118955887_118955888insCTTTTTTTTTTTTTTTT , CM000673.1:g.118955887_118955888insCTTTTTTTTTTTTTTTT	GRCh37
NC_000011.8:g.118461097_118461098insCTTTTTTTTTTTTTTTT	NCBI36
NG_008093.1:g.5301_5302insCTTTTTTTTTTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000442944.7:c.33+111_33+112insCTTTTTTTTTTTTTTTT	ENSP00000392041.3:n.33+111_33+112insCTTTTTTTTTTTTTTTT
ENST00000534956.2:n.36+111_36+112insCTTTTTTTTTTTTTTTT
ENST00000536813.6:c.-102+111_-102+112insCTTTTTTTTTTTTTTTT	ENSP00000438726.2:n.-102+111_-102+112insCTTTTTTTTTTTTTTTT
ENST00000546302.6:c.33+111_33+112insCTTTTTTTTTTTTTTTT	ENSP00000445599.1:n.33+111_33+112insCTTTTTTTTTTTTTTTT
ENST00000640813.1:c.-19+111_-19+112insCTTTTTTTTTTTTTTTT	ENSP00000491061.1:n.-19+111_-19+112insCTTTTTTTTTTTTTTTT
ENST00000648026.1:c.27+111_27+112insCTTTTTTTTTTTTTTTT	ENSP00000498044.1:n.27+111_27+112insCTTTTTTTTTTTTTTTT
ENST00000649868.1:c.33+111_33+112insCTTTTTTTTTTTTTTTT	ENSP00000497548.1:n.33+111_33+112insCTTTTTTTTTTTTTTTT
ENST00000652429.1:c.33+111_33+112insCTTTTTTTTTTTTTTTT MANE Select	ENSP00000498786.1:n.33+111_33+112insCTTTTTTTTTTTTTTTT
ENST00000278715.7:c.33+111_33+112insCTTTTTTTTTTTTTTTT	ENSP00000278715.3:n.33+111_33+112insCTTTTTTTTTTTTTTTT
ENST00000442944.6:c.-102+111_-102+112insCTTTTTTTTTTTTTTTT	ENSP00000392041.2:n.-102+111_-102+112insCTTTTTTTTTTTTTTTT
ENST00000535793.5:c.33+111_33+112insCTTTTTTTTTTTTTTTT	ENSP00000439904.1:n.33+111_33+112insCTTTTTTTTTTTTTTTT
ENST00000536185.5:n.201+111_201+112insCTTTTTTTTTTTTTTTT
ENST00000536813.5:c.33+111_33+112insCTTTTTTTTTTTTTTTT	ENSP00000438726.1:n.33+111_33+112insCTTTTTTTTTTTTTTTT
ENST00000537841.5:c.-19+20_-19+21insCTTTTTTTTTTTTTTTT	ENSP00000444730.1:n.-19+20_-19+21insCTTTTTTTTTTTTTTTT
ENST00000542044.5:n.158+111_158+112insCTTTTTTTTTTTTTTTT
ENST00000542729.5:c.-19+20_-19+21insCTTTTTTTTTTTTTTTT	ENSP00000443058.1:n.-19+20_-19+21insCTTTTTTTTTTTTTTTT
ENST00000542822.5:c.124+20_124+21insCTTTTTTTTTTTTTTTT	ENSP00000444817.1:n.124+20_124+21insCTTTTTTTTTTTTTTTT
ENST00000543090.5:c.33+111_33+112insCTTTTTTTTTTTTTTTT	ENSP00000445429.1:n.33+111_33+112insCTTTTTTTTTTTTTTTT
ENST00000543821.5:n.179+111_179+112insCTTTTTTTTTTTTTTTT
ENST00000544387.5:c.33+111_33+112insCTTTTTTTTTTTTTTTT	ENSP00000438424.1:n.33+111_33+112insCTTTTTTTTTTTTTTTT
ENST00000545621.5:c.33+111_33+112insCTTTTTTTTTTTTTTTT	ENSP00000444849.1:n.33+111_33+112insCTTTTTTTTTTTTTTTT
ENST00000545901.5:n.186+111_186+112insCTTTTTTTTTTTTTTTT
ENST00000546302.5:c.33+111_33+112insCTTTTTTTTTTTTTTTT	ENSP00000445599.1:n.33+111_33+112insCTTTTTTTTTTTTTTTT
NM_000190.3:c.33+111_33+112insCTTTTTTTTTTTTTTTT	NP_000181.2:n.33+111_33+112insCTTTTTTTTTTTTTTTT
NM_001258208.1:c.33+111_33+112insCTTTTTTTTTTTTTTTT	NP_001245137.1:n.33+111_33+112insCTTTTTTTTTTTTTTTT
NM_001258209.1:c.-19+20_-19+21insCTTTTTTTTTTTTTTTT	NP_001245138.1:n.-19+20_-19+21insCTTTTTTTTTTTTTTTT
XM_005271531.1:c.-19+20_-19+21insCTTTTTTTTTTTTTTTT	XP_005271588.1:n.-19+20_-19+21insCTTTTTTTTTTTTTTTT
XM_005271532.1:c.-19+44_-19+45insCTTTTTTTTTTTTTTTT	XP_005271589.1:n.-19+44_-19+45insCTTTTTTTTTTTTTTTT
XM_005271533.2:c.33+111_33+112insCTTTTTTTTTTTTTTTT	XP_005271590.1:n.33+111_33+112insCTTTTTTTTTTTTTTTT
NM_000190.4:c.33+111_33+112insCTTTTTTTTTTTTTTTT MANE Select	NP_000181.2:n.33+111_33+112insCTTTTTTTTTTTTTTTT
XM_005271533.3:c.33+111_33+112insCTTTTTTTTTTTTTTTT	XP_005271590.1:n.33+111_33+112insCTTTTTTTTTTTTTTTT
XM_024448460.1:c.33+111_33+112insCTTTTTTTTTTTTTTTT	XP_024304228.1:n.33+111_33+112insCTTTTTTTTTTTTTTTT
NM_001258208.2:c.33+111_33+112insCTTTTTTTTTTTTTTTT	NP_001245137.1:n.33+111_33+112insCTTTTTTTTTTTTTTTT
NM_001258209.2:c.-19+20_-19+21insCTTTTTTTTTTTTTTTT	NP_001245138.1:n.-19+20_-19+21insCTTTTTTTTTTTTTTTT