Canonical Allele Identifier: CA2003782800
Gene: HMBS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119089742C= , CM000673.2:g.119089742C= GRCh38
NC_000011.9:g.118960452C= , CM000673.1:g.118960452C= GRCh37
NC_000011.8:g.118465662C= NCBI36
NG_008093.1:g.9866C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000686218.1:c.161C= ENSP00000509288.1:p.Thr54=
ENST00000686690.1:n.947C=
ENST00000691144.1:n.2067C=
ENST00000691249.1:n.910C=
ENST00000442944.7:c.308C= ENSP00000392041.3:p.Thr103=
ENST00000534956.2:n.275C=
ENST00000536813.6:c.275C= ENSP00000438726.2:p.Thr92=
ENST00000546302.6:c.267-248C= ENSP00000445599.1:n.267-248C=
ENST00000640813.1:c.275C= ENSP00000491061.1:p.Thr92=
ENST00000648026.1:c.320C= ENSP00000498044.1:p.Thr107=
ENST00000648374.1:c.275C= ENSP00000497255.1:p.Thr92=
ENST00000648488.1:c.275C= ENSP00000498079.1:p.Thr92=
ENST00000649823.1:n.543C=
ENST00000649868.1:c.*34C= ENSP00000497548.1:n.*34C=
ENST00000650101.1:c.257C= ENSP00000496970.1:p.Thr86=
ENST00000650307.1:n.1152C=
ENST00000652429.1:c.326C= MANE Select ENSP00000498786.1:p.Thr109=
ENST00000278715.7:c.326C= ENSP00000278715.3:p.Thr109=
ENST00000392841.1:c.275C= ENSP00000376584.1:p.Thr92=
ENST00000442944.6:c.275C= ENSP00000392041.2:p.Thr92=
ENST00000534956.1:n.242C=
ENST00000535253.5:c.275C= ENSP00000442079.1:p.Thr92=
ENST00000535793.5:c.*221C= ENSP00000439904.1:n.*221C=
ENST00000536813.5:c.308C= ENSP00000438726.1:p.Thr103=
ENST00000537841.5:c.275C= ENSP00000444730.1:p.Thr92=
ENST00000539986.5:c.275C= ENSP00000440092.1:p.Thr92=
ENST00000542044.5:n.771C=
ENST00000542345.5:n.464C=
ENST00000542729.5:c.275C= ENSP00000443058.1:p.Thr92=
ENST00000542822.5:c.*262C= ENSP00000444817.1:n.*262C=
ENST00000543090.5:c.272C= ENSP00000445429.1:p.Thr91=
ENST00000543543.5:n.561C=
ENST00000543821.5:n.472C=
ENST00000544360.5:n.294C=
ENST00000544387.5:c.326C= ENSP00000438424.1:p.Thr109=
ENST00000545621.5:c.*221C= ENSP00000444849.1:n.*221C=
ENST00000546226.5:n.385C=
ENST00000546302.5:c.267-248C= ENSP00000445599.1:n.267-248C=
NM_000190.3:c.326C= NP_000181.2:p.Thr109=
NM_001024382.1:c.275C= NP_001019553.1:p.Thr92=
NM_001258208.1:c.326C= NP_001245137.1:p.Thr109=
NM_001258209.1:c.275C= NP_001245138.1:p.Thr92=
XM_005271531.1:c.275C= XP_005271588.1:p.Thr92=
XM_005271532.1:c.275C= XP_005271589.1:p.Thr92=
XM_005271533.2:c.272C= XP_005271590.1:p.Thr91=
XM_011542796.1:c.161C= XP_011541098.1:p.Thr54=
NM_000190.4:c.326C= MANE Select NP_000181.2:p.Thr109=
NM_001024382.2:c.275C= NP_001019553.1:p.Thr92=
XM_005271533.3:c.272C= XP_005271590.1:p.Thr91=
XM_017017629.1:c.275C= XP_016873118.1:p.Thr92=
XM_024448460.1:c.272C= XP_024304228.1:p.Thr91=
NM_001258208.2:c.326C= NP_001245137.1:p.Thr109=
NM_001258209.2:c.275C= NP_001245138.1:p.Thr92=