Canonical Allele Identifier: CA2003782512
Gene: HMBS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119089122A= , CM000673.2:g.119089122A= GRCh38
NC_000011.9:g.118959832A= , CM000673.1:g.118959832A= GRCh37
NC_000011.8:g.118465042A= NCBI36
NG_008093.1:g.9246A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000686218.1:c.36A= ENSP00000509288.1:p.Ala12=
ENST00000686690.1:n.737A=
ENST00000691144.1:n.1857A=
ENST00000691249.1:n.785A=
ENST00000442944.7:c.183A= ENSP00000392041.3:p.Ala61=
ENST00000534956.2:n.150A=
ENST00000536813.6:c.150A= ENSP00000438726.2:p.Ala50=
ENST00000546302.6:c.201A= ENSP00000445599.1:p.Ala67=
ENST00000640813.1:c.150A= ENSP00000491061.1:p.Ala50=
ENST00000648026.1:c.195A= ENSP00000498044.1:p.Ala65=
ENST00000648374.1:c.150A= ENSP00000497255.1:p.Ala50=
ENST00000648488.1:c.150A= ENSP00000498079.1:p.Ala50=
ENST00000649823.1:n.418A=
ENST00000649868.1:c.56A= ENSP00000497548.1:p.His19=
ENST00000650101.1:c.132A= ENSP00000496970.1:p.Ala44=
ENST00000650307.1:n.1027A=
ENST00000652429.1:c.201A= MANE Select ENSP00000498786.1:p.Ala67=
ENST00000278715.7:c.201A= ENSP00000278715.3:p.Ala67=
ENST00000392841.1:c.150A= ENSP00000376584.1:p.Ala50=
ENST00000442944.6:c.150A= ENSP00000392041.2:p.Ala50=
ENST00000534956.1:n.117A=
ENST00000535253.5:c.150A= ENSP00000442079.1:p.Ala50=
ENST00000535793.5:c.*96A= ENSP00000439904.1:n.*96A=
ENST00000536185.5:n.329-95A=
ENST00000536813.5:c.183A= ENSP00000438726.1:p.Ala61=
ENST00000537841.5:c.150A= ENSP00000444730.1:p.Ala50=
ENST00000539986.5:c.150A= ENSP00000440092.1:p.Ala50=
ENST00000542044.5:n.646A=
ENST00000542345.5:n.339A=
ENST00000542729.5:c.150A= ENSP00000443058.1:p.Ala50=
ENST00000542822.5:c.*147-95A= ENSP00000444817.1:n.*147-95A=
ENST00000543090.5:c.147A= ENSP00000445429.1:p.Ala49=
ENST00000543543.5:n.436A=
ENST00000543821.5:n.347A=
ENST00000544360.5:n.169A=
ENST00000544387.5:c.201A= ENSP00000438424.1:p.Ala67=
ENST00000545621.5:c.*96A= ENSP00000444849.1:n.*96A=
ENST00000546226.5:n.260A=
ENST00000546302.5:c.201A= ENSP00000445599.1:p.Ala67=
NM_000190.3:c.201A= NP_000181.2:p.Ala67=
NM_001024382.1:c.150A= NP_001019553.1:p.Ala50=
NM_001258208.1:c.201A= NP_001245137.1:p.Ala67=
NM_001258209.1:c.150A= NP_001245138.1:p.Ala50=
XM_005271531.1:c.150A= XP_005271588.1:p.Ala50=
XM_005271532.1:c.150A= XP_005271589.1:p.Ala50=
XM_005271533.2:c.147A= XP_005271590.1:p.Ala49=
XM_011542796.1:c.36A= XP_011541098.1:p.Ala12=
NM_000190.4:c.201A= MANE Select NP_000181.2:p.Ala67=
NM_001024382.2:c.150A= NP_001019553.1:p.Ala50=
XM_005271533.3:c.147A= XP_005271590.1:p.Ala49=
XM_017017629.1:c.150A= XP_016873118.1:p.Ala50=
XM_024448460.1:c.147A= XP_024304228.1:p.Ala49=
NM_001258208.2:c.201A= NP_001245137.1:p.Ala67=
NM_001258209.2:c.150A= NP_001245138.1:p.Ala50=