Canonical Allele Identifier: CA2616352744

Gene: HMBS

Linked Data

• gnomAD v4: 11-119085172-C-CTTTTCTTTTTTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119085176_119085177insCTTTTTTTTTTTTT , CM000673.2:g.119085176_119085177insCTTTTTTTTTTTTT	GRCh38
NC_000011.9:g.118955886_118955887insCTTTTTTTTTTTTT , CM000673.1:g.118955886_118955887insCTTTTTTTTTTTTT	GRCh37
NC_000011.8:g.118461096_118461097insCTTTTTTTTTTTTT	NCBI36
NG_008093.1:g.5300_5301insCTTTTTTTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000442944.7:c.33+110_33+111insCTTTTTTTTTTTTT	ENSP00000392041.3:n.33+110_33+111insCTTTTTTTTTTTTT
ENST00000534956.2:n.36+110_36+111insCTTTTTTTTTTTTT
ENST00000536813.6:c.-102+110_-102+111insCTTTTTTTTTTTTT	ENSP00000438726.2:n.-102+110_-102+111insCTTTTTTTTTTTTT
ENST00000546302.6:c.33+110_33+111insCTTTTTTTTTTTTT	ENSP00000445599.1:n.33+110_33+111insCTTTTTTTTTTTTT
ENST00000640813.1:c.-19+110_-19+111insCTTTTTTTTTTTTT	ENSP00000491061.1:n.-19+110_-19+111insCTTTTTTTTTTTTT
ENST00000648026.1:c.27+110_27+111insCTTTTTTTTTTTTT	ENSP00000498044.1:n.27+110_27+111insCTTTTTTTTTTTTT
ENST00000649868.1:c.33+110_33+111insCTTTTTTTTTTTTT	ENSP00000497548.1:n.33+110_33+111insCTTTTTTTTTTTTT
ENST00000652429.1:c.33+110_33+111insCTTTTTTTTTTTTT MANE Select	ENSP00000498786.1:n.33+110_33+111insCTTTTTTTTTTTTT
ENST00000278715.7:c.33+110_33+111insCTTTTTTTTTTTTT	ENSP00000278715.3:n.33+110_33+111insCTTTTTTTTTTTTT
ENST00000442944.6:c.-102+110_-102+111insCTTTTTTTTTTTTT	ENSP00000392041.2:n.-102+110_-102+111insCTTTTTTTTTTTTT
ENST00000535793.5:c.33+110_33+111insCTTTTTTTTTTTTT	ENSP00000439904.1:n.33+110_33+111insCTTTTTTTTTTTTT
ENST00000536185.5:n.201+110_201+111insCTTTTTTTTTTTTT
ENST00000536813.5:c.33+110_33+111insCTTTTTTTTTTTTT	ENSP00000438726.1:n.33+110_33+111insCTTTTTTTTTTTTT
ENST00000537841.5:c.-19+19_-19+20insCTTTTTTTTTTTTT	ENSP00000444730.1:n.-19+19_-19+20insCTTTTTTTTTTTTT
ENST00000542044.5:n.158+110_158+111insCTTTTTTTTTTTTT
ENST00000542729.5:c.-19+19_-19+20insCTTTTTTTTTTTTT	ENSP00000443058.1:n.-19+19_-19+20insCTTTTTTTTTTTTT
ENST00000542822.5:c.124+19_124+20insCTTTTTTTTTTTTT	ENSP00000444817.1:n.124+19_124+20insCTTTTTTTTTTTTT
ENST00000543090.5:c.33+110_33+111insCTTTTTTTTTTTTT	ENSP00000445429.1:n.33+110_33+111insCTTTTTTTTTTTTT
ENST00000543821.5:n.179+110_179+111insCTTTTTTTTTTTTT
ENST00000544387.5:c.33+110_33+111insCTTTTTTTTTTTTT	ENSP00000438424.1:n.33+110_33+111insCTTTTTTTTTTTTT
ENST00000545621.5:c.33+110_33+111insCTTTTTTTTTTTTT	ENSP00000444849.1:n.33+110_33+111insCTTTTTTTTTTTTT
ENST00000545901.5:n.186+110_186+111insCTTTTTTTTTTTTT
ENST00000546302.5:c.33+110_33+111insCTTTTTTTTTTTTT	ENSP00000445599.1:n.33+110_33+111insCTTTTTTTTTTTTT
NM_000190.3:c.33+110_33+111insCTTTTTTTTTTTTT	NP_000181.2:n.33+110_33+111insCTTTTTTTTTTTTT
NM_001258208.1:c.33+110_33+111insCTTTTTTTTTTTTT	NP_001245137.1:n.33+110_33+111insCTTTTTTTTTTTTT
NM_001258209.1:c.-19+19_-19+20insCTTTTTTTTTTTTT	NP_001245138.1:n.-19+19_-19+20insCTTTTTTTTTTTTT
XM_005271531.1:c.-19+19_-19+20insCTTTTTTTTTTTTT	XP_005271588.1:n.-19+19_-19+20insCTTTTTTTTTTTTT
XM_005271532.1:c.-19+43_-19+44insCTTTTTTTTTTTTT	XP_005271589.1:n.-19+43_-19+44insCTTTTTTTTTTTTT
XM_005271533.2:c.33+110_33+111insCTTTTTTTTTTTTT	XP_005271590.1:n.33+110_33+111insCTTTTTTTTTTTTT
NM_000190.4:c.33+110_33+111insCTTTTTTTTTTTTT MANE Select	NP_000181.2:n.33+110_33+111insCTTTTTTTTTTTTT
XM_005271533.3:c.33+110_33+111insCTTTTTTTTTTTTT	XP_005271590.1:n.33+110_33+111insCTTTTTTTTTTTTT
XM_024448460.1:c.33+110_33+111insCTTTTTTTTTTTTT	XP_024304228.1:n.33+110_33+111insCTTTTTTTTTTTTT
NM_001258208.2:c.33+110_33+111insCTTTTTTTTTTTTT	NP_001245137.1:n.33+110_33+111insCTTTTTTTTTTTTT
NM_001258209.2:c.-19+19_-19+20insCTTTTTTTTTTTTT	NP_001245138.1:n.-19+19_-19+20insCTTTTTTTTTTTTT