Canonical Allele Identifier: CA2003780680

Gene: HMBS

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119085191_119085202delinsTTTTTTTTTTTG , CM000673.2:g.119085191_119085202delinsTTTTTTTTTTTG	GRCh38
NC_000011.9:g.118955901_118955912delinsTTTTTTTTTTTG , CM000673.1:g.118955901_118955912delinsTTTTTTTTTTTG	GRCh37
NC_000011.8:g.118461111_118461122delinsTTTTTTTTTTTG	NCBI36
NG_008093.1:g.5315_5326delinsTTTTTTTTTTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000442944.7:c.33+125_33+136delinsTTTTTTTTTTTG	ENSP00000392041.3:n.33+125_33+136delinsTTTTTTTTTTTG
ENST00000534956.2:n.36+125_36+136delinsTTTTTTTTTTTG
ENST00000536813.6:c.-102+125_-102+136delinsTTTTTTTTTTTG	ENSP00000438726.2:n.-102+125_-102+136delinsTTTTTTTTTTTG
ENST00000546302.6:c.33+125_33+136delinsTTTTTTTTTTTG	ENSP00000445599.1:n.33+125_33+136delinsTTTTTTTTTTTG
ENST00000640813.1:c.-19+125_-19+136delinsTTTTTTTTTTTG	ENSP00000491061.1:n.-19+125_-19+136delinsTTTTTTTTTTTG
ENST00000648026.1:c.27+125_27+136delinsTTTTTTTTTTTG	ENSP00000498044.1:n.27+125_27+136delinsTTTTTTTTTTTG
ENST00000649868.1:c.33+125_33+136delinsTTTTTTTTTTTG	ENSP00000497548.1:n.33+125_33+136delinsTTTTTTTTTTTG
ENST00000652429.1:c.33+125_33+136delinsTTTTTTTTTTTG MANE Select	ENSP00000498786.1:n.33+125_33+136delinsTTTTTTTTTTTG
ENST00000278715.7:c.33+125_33+136delinsTTTTTTTTTTTG	ENSP00000278715.3:n.33+125_33+136delinsTTTTTTTTTTTG
ENST00000442944.6:c.-102+125_-102+136delinsTTTTTTTTTTTG	ENSP00000392041.2:n.-102+125_-102+136delinsTTTTTTTTTTTG
ENST00000535793.5:c.33+125_33+136delinsTTTTTTTTTTTG	ENSP00000439904.1:n.33+125_33+136delinsTTTTTTTTTTTG
ENST00000536185.5:n.201+125_201+136delinsTTTTTTTTTTTG
ENST00000536813.5:c.33+125_33+136delinsTTTTTTTTTTTG	ENSP00000438726.1:n.33+125_33+136delinsTTTTTTTTTTTG
ENST00000537841.5:c.-19+34_-19+45delinsTTTTTTTTTTTG	ENSP00000444730.1:n.-19+34_-19+45delinsTTTTTTTTTTTG
ENST00000542044.5:n.158+125_158+136delinsTTTTTTTTTTTG
ENST00000542729.5:c.-19+34_-19+45delinsTTTTTTTTTTTG	ENSP00000443058.1:n.-19+34_-19+45delinsTTTTTTTTTTTG
ENST00000542822.5:c.124+34_124+45delinsTTTTTTTTTTTG	ENSP00000444817.1:n.124+34_124+45delinsTTTTTTTTTTTG
ENST00000543090.5:c.33+125_33+136delinsTTTTTTTTTTTG	ENSP00000445429.1:n.33+125_33+136delinsTTTTTTTTTTTG
ENST00000543821.5:n.179+125_179+136delinsTTTTTTTTTTTG
ENST00000544387.5:c.33+125_33+136delinsTTTTTTTTTTTG	ENSP00000438424.1:n.33+125_33+136delinsTTTTTTTTTTTG
ENST00000545621.5:c.33+125_33+136delinsTTTTTTTTTTTG	ENSP00000444849.1:n.33+125_33+136delinsTTTTTTTTTTTG
ENST00000545901.5:n.186+125_186+136delinsTTTTTTTTTTTG
ENST00000546302.5:c.33+125_33+136delinsTTTTTTTTTTTG	ENSP00000445599.1:n.33+125_33+136delinsTTTTTTTTTTTG
NM_000190.3:c.33+125_33+136delinsTTTTTTTTTTTG	NP_000181.2:n.33+125_33+136delinsTTTTTTTTTTTG
NM_001258208.1:c.33+125_33+136delinsTTTTTTTTTTTG	NP_001245137.1:n.33+125_33+136delinsTTTTTTTTTTTG
NM_001258209.1:c.-19+34_-19+45delinsTTTTTTTTTTTG	NP_001245138.1:n.-19+34_-19+45delinsTTTTTTTTTTTG
XM_005271531.1:c.-19+34_-19+45delinsTTTTTTTTTTTG	XP_005271588.1:n.-19+34_-19+45delinsTTTTTTTTTTTG
XM_005271532.1:c.-19+58_-19+69delinsTTTTTTTTTTTG	XP_005271589.1:n.-19+58_-19+69delinsTTTTTTTTTTTG
XM_005271533.2:c.33+125_33+136delinsTTTTTTTTTTTG	XP_005271590.1:n.33+125_33+136delinsTTTTTTTTTTTG
NM_000190.4:c.33+125_33+136delinsTTTTTTTTTTTG MANE Select	NP_000181.2:n.33+125_33+136delinsTTTTTTTTTTTG
XM_005271533.3:c.33+125_33+136delinsTTTTTTTTTTTG	XP_005271590.1:n.33+125_33+136delinsTTTTTTTTTTTG
XM_024448460.1:c.33+125_33+136delinsTTTTTTTTTTTG	XP_024304228.1:n.33+125_33+136delinsTTTTTTTTTTTG
NM_001258208.2:c.33+125_33+136delinsTTTTTTTTTTTG	NP_001245137.1:n.33+125_33+136delinsTTTTTTTTTTTG
NM_001258209.2:c.-19+34_-19+45delinsTTTTTTTTTTTG	NP_001245138.1:n.-19+34_-19+45delinsTTTTTTTTTTTG