Canonical Allele Identifier: CA2003782500
Gene: HMBS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119089088T= , CM000673.2:g.119089088T= GRCh38
NC_000011.9:g.118959798T= , CM000673.1:g.118959798T= GRCh37
NC_000011.8:g.118465008T= NCBI36
NG_008093.1:g.9212T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000686218.1:c.2T= ENSP00000509288.1:p.Met1=
ENST00000686690.1:n.703T=
ENST00000691144.1:n.1823T=
ENST00000691249.1:n.751T=
ENST00000442944.7:c.161-12T= ENSP00000392041.3:n.161-12T=
ENST00000534956.2:n.116T=
ENST00000536813.6:c.116T= ENSP00000438726.2:p.Met39=
ENST00000546302.6:c.167T= ENSP00000445599.1:p.Met56=
ENST00000640813.1:c.116T= ENSP00000491061.1:p.Met39=
ENST00000648026.1:c.161T= ENSP00000498044.1:p.Met54=
ENST00000648374.1:c.116T= ENSP00000497255.1:p.Met39=
ENST00000648488.1:c.116T= ENSP00000498079.1:p.Met39=
ENST00000649823.1:n.384T=
ENST00000649868.1:c.34-12T= ENSP00000497548.1:n.34-12T=
ENST00000650101.1:c.110-12T= ENSP00000496970.1:n.110-12T=
ENST00000650307.1:n.993T=
ENST00000652429.1:c.167T= MANE Select ENSP00000498786.1:p.Met56=
ENST00000278715.7:c.167T= ENSP00000278715.3:p.Met56=
ENST00000392841.1:c.116T= ENSP00000376584.1:p.Met39=
ENST00000442944.6:c.116T= ENSP00000392041.2:p.Met39=
ENST00000534956.1:n.83T=
ENST00000535253.5:c.116T= ENSP00000442079.1:p.Met39=
ENST00000535793.5:c.*62T= ENSP00000439904.1:n.*62T=
ENST00000536185.5:n.329-129T=
ENST00000536813.5:c.161-12T= ENSP00000438726.1:n.161-12T=
ENST00000537841.5:c.116T= ENSP00000444730.1:p.Met39=
ENST00000539986.5:c.116T= ENSP00000440092.1:p.Met39=
ENST00000542044.5:n.612T=
ENST00000542345.5:n.305T=
ENST00000542729.5:c.116T= ENSP00000443058.1:p.Met39=
ENST00000542822.5:c.*147-129T= ENSP00000444817.1:n.*147-129T=
ENST00000543090.5:c.113T= ENSP00000445429.1:p.Met38=
ENST00000543543.5:n.402T=
ENST00000543821.5:n.313T=
ENST00000544360.5:n.135T=
ENST00000544387.5:c.167T= ENSP00000438424.1:p.Met56=
ENST00000545621.5:c.*62T= ENSP00000444849.1:n.*62T=
ENST00000546226.5:n.226T=
ENST00000546302.5:c.167T= ENSP00000445599.1:p.Met56=
NM_000190.3:c.167T= NP_000181.2:p.Met56=
NM_001024382.1:c.116T= NP_001019553.1:p.Met39=
NM_001258208.1:c.167T= NP_001245137.1:p.Met56=
NM_001258209.1:c.116T= NP_001245138.1:p.Met39=
XM_005271531.1:c.116T= XP_005271588.1:p.Met39=
XM_005271532.1:c.116T= XP_005271589.1:p.Met39=
XM_005271533.2:c.113T= XP_005271590.1:p.Met38=
XM_011542796.1:c.2T= XP_011541098.1:p.Met1=
NM_000190.4:c.167T= MANE Select NP_000181.2:p.Met56=
NM_001024382.2:c.116T= NP_001019553.1:p.Met39=
XM_005271533.3:c.113T= XP_005271590.1:p.Met38=
XM_017017629.1:c.116T= XP_016873118.1:p.Met39=
XM_024448460.1:c.113T= XP_024304228.1:p.Met38=
NM_001258208.2:c.167T= NP_001245137.1:p.Met56=
NM_001258209.2:c.116T= NP_001245138.1:p.Met39=