Canonical Allele Identifier: CA2003780690

Gene: HMBS

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119085198_119085202delinsTTTTG , CM000673.2:g.119085198_119085202delinsTTTTG	GRCh38
NC_000011.9:g.118955908_118955912delinsTTTTG , CM000673.1:g.118955908_118955912delinsTTTTG	GRCh37
NC_000011.8:g.118461118_118461122delinsTTTTG	NCBI36
NG_008093.1:g.5322_5326delinsTTTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000442944.7:c.33+132_33+136delinsTTTTG	ENSP00000392041.3:n.33+132_33+136delinsTTTTG
ENST00000534956.2:n.36+132_36+136delinsTTTTG
ENST00000536813.6:c.-102+132_-102+136delinsTTTTG	ENSP00000438726.2:n.-102+132_-102+136delinsTTTTG
ENST00000546302.6:c.33+132_33+136delinsTTTTG	ENSP00000445599.1:n.33+132_33+136delinsTTTTG
ENST00000640813.1:c.-19+132_-19+136delinsTTTTG	ENSP00000491061.1:n.-19+132_-19+136delinsTTTTG
ENST00000648026.1:c.27+132_27+136delinsTTTTG	ENSP00000498044.1:n.27+132_27+136delinsTTTTG
ENST00000649868.1:c.33+132_33+136delinsTTTTG	ENSP00000497548.1:n.33+132_33+136delinsTTTTG
ENST00000652429.1:c.33+132_33+136delinsTTTTG MANE Select	ENSP00000498786.1:n.33+132_33+136delinsTTTTG
ENST00000278715.7:c.33+132_33+136delinsTTTTG	ENSP00000278715.3:n.33+132_33+136delinsTTTTG
ENST00000442944.6:c.-102+132_-102+136delinsTTTTG	ENSP00000392041.2:n.-102+132_-102+136delinsTTTTG
ENST00000535793.5:c.33+132_33+136delinsTTTTG	ENSP00000439904.1:n.33+132_33+136delinsTTTTG
ENST00000536185.5:n.201+132_201+136delinsTTTTG
ENST00000536813.5:c.33+132_33+136delinsTTTTG	ENSP00000438726.1:n.33+132_33+136delinsTTTTG
ENST00000537841.5:c.-19+41_-19+45delinsTTTTG	ENSP00000444730.1:n.-19+41_-19+45delinsTTTTG
ENST00000542044.5:n.158+132_158+136delinsTTTTG
ENST00000542729.5:c.-19+41_-19+45delinsTTTTG	ENSP00000443058.1:n.-19+41_-19+45delinsTTTTG
ENST00000542822.5:c.124+41_124+45delinsTTTTG	ENSP00000444817.1:n.124+41_124+45delinsTTTTG
ENST00000543090.5:c.33+132_33+136delinsTTTTG	ENSP00000445429.1:n.33+132_33+136delinsTTTTG
ENST00000543821.5:n.179+132_179+136delinsTTTTG
ENST00000544387.5:c.33+132_33+136delinsTTTTG	ENSP00000438424.1:n.33+132_33+136delinsTTTTG
ENST00000545621.5:c.33+132_33+136delinsTTTTG	ENSP00000444849.1:n.33+132_33+136delinsTTTTG
ENST00000545901.5:n.186+132_186+136delinsTTTTG
ENST00000546302.5:c.33+132_33+136delinsTTTTG	ENSP00000445599.1:n.33+132_33+136delinsTTTTG
NM_000190.3:c.33+132_33+136delinsTTTTG	NP_000181.2:n.33+132_33+136delinsTTTTG
NM_001258208.1:c.33+132_33+136delinsTTTTG	NP_001245137.1:n.33+132_33+136delinsTTTTG
NM_001258209.1:c.-19+41_-19+45delinsTTTTG	NP_001245138.1:n.-19+41_-19+45delinsTTTTG
XM_005271531.1:c.-19+41_-19+45delinsTTTTG	XP_005271588.1:n.-19+41_-19+45delinsTTTTG
XM_005271532.1:c.-19+65_-19+69delinsTTTTG	XP_005271589.1:n.-19+65_-19+69delinsTTTTG
XM_005271533.2:c.33+132_33+136delinsTTTTG	XP_005271590.1:n.33+132_33+136delinsTTTTG
NM_000190.4:c.33+132_33+136delinsTTTTG MANE Select	NP_000181.2:n.33+132_33+136delinsTTTTG
XM_005271533.3:c.33+132_33+136delinsTTTTG	XP_005271590.1:n.33+132_33+136delinsTTTTG
XM_024448460.1:c.33+132_33+136delinsTTTTG	XP_024304228.1:n.33+132_33+136delinsTTTTG
NM_001258208.2:c.33+132_33+136delinsTTTTG	NP_001245137.1:n.33+132_33+136delinsTTTTG
NM_001258209.2:c.-19+41_-19+45delinsTTTTG	NP_001245138.1:n.-19+41_-19+45delinsTTTTG