Canonical Allele Identifier: CA2616352563

Gene: HMBS

Linked Data

• gnomAD v4: 11-119084979-C-CG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119084983dup , CM000673.2:g.119084983dup	GRCh38
NC_000011.9:g.118955693dup , CM000673.1:g.118955693dup	GRCh37
NC_000011.8:g.118460903dup	NCBI36
NG_008093.1:g.5107dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000442944.7:c.-51dup	ENSP00000392041.3:n.-51dup
ENST00000536813.6:c.-185dup	ENSP00000438726.2:n.-185dup
ENST00000546302.6:c.-51dup	ENSP00000445599.1:n.-51dup
ENST00000640813.1:c.-102dup	ENSP00000491061.1:n.-102dup
ENST00000652429.1:c.-51dup MANE Select	ENSP00000498786.1:n.-51dup
ENST00000278715.7:c.-51dup	ENSP00000278715.3:n.-51dup
ENST00000442944.6:c.-185dup	ENSP00000392041.2:n.-185dup
ENST00000535793.5:c.-51dup	ENSP00000439904.1:n.-51dup
ENST00000536185.5:n.118dup
ENST00000536813.5:c.-51dup	ENSP00000438726.1:n.-51dup
ENST00000537841.5:c.-193dup	ENSP00000444730.1:n.-193dup
ENST00000542044.5:n.75dup
ENST00000542729.5:c.-193dup	ENSP00000443058.1:n.-193dup
ENST00000542822.5:c.-51dup	ENSP00000444817.1:n.-51dup
ENST00000543090.5:c.-51dup	ENSP00000445429.1:n.-51dup
ENST00000543821.5:n.96dup
ENST00000544387.5:c.-51dup	ENSP00000438424.1:n.-51dup
ENST00000545621.5:c.-51dup	ENSP00000444849.1:n.-51dup
ENST00000545901.5:n.103dup
ENST00000546302.5:c.-51dup	ENSP00000445599.1:n.-51dup
NM_000190.3:c.-51dup	NP_000181.2:n.-51dup
NM_001258208.1:c.-51dup	NP_001245137.1:n.-51dup
NM_001258209.1:c.-193dup	NP_001245138.1:n.-193dup
XM_005271531.1:c.-193dup	XP_005271588.1:n.-193dup
XM_005271532.1:c.-169dup	XP_005271589.1:n.-169dup
XM_005271533.2:c.-51dup	XP_005271590.1:n.-51dup
NM_000190.4:c.-51dup MANE Select	NP_000181.2:n.-51dup
XM_005271533.3:c.-51dup	XP_005271590.1:n.-51dup
XM_024448460.1:c.-51dup	XP_024304228.1:n.-51dup
NM_001258208.2:c.-51dup	NP_001245137.1:n.-51dup
NM_001258209.2:c.-193dup	NP_001245138.1:n.-193dup