Canonical Allele Identifier: CA2003780679

Gene: HMBS

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119085189_119085202delinsTTTTTTTTTTTTTG , CM000673.2:g.119085189_119085202delinsTTTTTTTTTTTTTG	GRCh38
NC_000011.9:g.118955899_118955912delinsTTTTTTTTTTTTTG , CM000673.1:g.118955899_118955912delinsTTTTTTTTTTTTTG	GRCh37
NC_000011.8:g.118461109_118461122delinsTTTTTTTTTTTTTG	NCBI36
NG_008093.1:g.5313_5326delinsTTTTTTTTTTTTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000442944.7:c.33+123_33+136delinsTTTTTTTTTTTTTG	ENSP00000392041.3:n.33+123_33+136delinsTTTTTTTTTTTTTG
ENST00000534956.2:n.36+123_36+136delinsTTTTTTTTTTTTTG
ENST00000536813.6:c.-102+123_-102+136delinsTTTTTTTTTTTTTG	ENSP00000438726.2:n.-102+123_-102+136delinsTTTTTTTTTTTTTG
ENST00000546302.6:c.33+123_33+136delinsTTTTTTTTTTTTTG	ENSP00000445599.1:n.33+123_33+136delinsTTTTTTTTTTTTTG
ENST00000640813.1:c.-19+123_-19+136delinsTTTTTTTTTTTTTG	ENSP00000491061.1:n.-19+123_-19+136delinsTTTTTTTTTTTTTG
ENST00000648026.1:c.27+123_27+136delinsTTTTTTTTTTTTTG	ENSP00000498044.1:n.27+123_27+136delinsTTTTTTTTTTTTTG
ENST00000649868.1:c.33+123_33+136delinsTTTTTTTTTTTTTG	ENSP00000497548.1:n.33+123_33+136delinsTTTTTTTTTTTTTG
ENST00000652429.1:c.33+123_33+136delinsTTTTTTTTTTTTTG MANE Select	ENSP00000498786.1:n.33+123_33+136delinsTTTTTTTTTTTTTG
ENST00000278715.7:c.33+123_33+136delinsTTTTTTTTTTTTTG	ENSP00000278715.3:n.33+123_33+136delinsTTTTTTTTTTTTTG
ENST00000442944.6:c.-102+123_-102+136delinsTTTTTTTTTTTTTG	ENSP00000392041.2:n.-102+123_-102+136delinsTTTTTTTTTTTTTG
ENST00000535793.5:c.33+123_33+136delinsTTTTTTTTTTTTTG	ENSP00000439904.1:n.33+123_33+136delinsTTTTTTTTTTTTTG
ENST00000536185.5:n.201+123_201+136delinsTTTTTTTTTTTTTG
ENST00000536813.5:c.33+123_33+136delinsTTTTTTTTTTTTTG	ENSP00000438726.1:n.33+123_33+136delinsTTTTTTTTTTTTTG
ENST00000537841.5:c.-19+32_-19+45delinsTTTTTTTTTTTTTG	ENSP00000444730.1:n.-19+32_-19+45delinsTTTTTTTTTTTTTG
ENST00000542044.5:n.158+123_158+136delinsTTTTTTTTTTTTTG
ENST00000542729.5:c.-19+32_-19+45delinsTTTTTTTTTTTTTG	ENSP00000443058.1:n.-19+32_-19+45delinsTTTTTTTTTTTTTG
ENST00000542822.5:c.124+32_124+45delinsTTTTTTTTTTTTTG	ENSP00000444817.1:n.124+32_124+45delinsTTTTTTTTTTTTTG
ENST00000543090.5:c.33+123_33+136delinsTTTTTTTTTTTTTG	ENSP00000445429.1:n.33+123_33+136delinsTTTTTTTTTTTTTG
ENST00000543821.5:n.179+123_179+136delinsTTTTTTTTTTTTTG
ENST00000544387.5:c.33+123_33+136delinsTTTTTTTTTTTTTG	ENSP00000438424.1:n.33+123_33+136delinsTTTTTTTTTTTTTG
ENST00000545621.5:c.33+123_33+136delinsTTTTTTTTTTTTTG	ENSP00000444849.1:n.33+123_33+136delinsTTTTTTTTTTTTTG
ENST00000545901.5:n.186+123_186+136delinsTTTTTTTTTTTTTG
ENST00000546302.5:c.33+123_33+136delinsTTTTTTTTTTTTTG	ENSP00000445599.1:n.33+123_33+136delinsTTTTTTTTTTTTTG
NM_000190.3:c.33+123_33+136delinsTTTTTTTTTTTTTG	NP_000181.2:n.33+123_33+136delinsTTTTTTTTTTTTTG
NM_001258208.1:c.33+123_33+136delinsTTTTTTTTTTTTTG	NP_001245137.1:n.33+123_33+136delinsTTTTTTTTTTTTTG
NM_001258209.1:c.-19+32_-19+45delinsTTTTTTTTTTTTTG	NP_001245138.1:n.-19+32_-19+45delinsTTTTTTTTTTTTTG
XM_005271531.1:c.-19+32_-19+45delinsTTTTTTTTTTTTTG	XP_005271588.1:n.-19+32_-19+45delinsTTTTTTTTTTTTTG
XM_005271532.1:c.-19+56_-19+69delinsTTTTTTTTTTTTTG	XP_005271589.1:n.-19+56_-19+69delinsTTTTTTTTTTTTTG
XM_005271533.2:c.33+123_33+136delinsTTTTTTTTTTTTTG	XP_005271590.1:n.33+123_33+136delinsTTTTTTTTTTTTTG
NM_000190.4:c.33+123_33+136delinsTTTTTTTTTTTTTG MANE Select	NP_000181.2:n.33+123_33+136delinsTTTTTTTTTTTTTG
XM_005271533.3:c.33+123_33+136delinsTTTTTTTTTTTTTG	XP_005271590.1:n.33+123_33+136delinsTTTTTTTTTTTTTG
XM_024448460.1:c.33+123_33+136delinsTTTTTTTTTTTTTG	XP_024304228.1:n.33+123_33+136delinsTTTTTTTTTTTTTG
NM_001258208.2:c.33+123_33+136delinsTTTTTTTTTTTTTG	NP_001245137.1:n.33+123_33+136delinsTTTTTTTTTTTTTG
NM_001258209.2:c.-19+32_-19+45delinsTTTTTTTTTTTTTG	NP_001245138.1:n.-19+32_-19+45delinsTTTTTTTTTTTTTG