Canonical Allele Identifier: CA2003790860
Gene: HMBS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119092129T= , CM000673.2:g.119092129T= GRCh38
NC_000011.9:g.118962839T= , CM000673.1:g.118962839T= GRCh37
NC_000011.8:g.118468049T= NCBI36
NG_008093.1:g.12253T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000686218.1:c.452T= ENSP00000509288.1:p.Leu151=
ENST00000691144.1:n.2358T=
ENST00000691249.1:n.1201T=
ENST00000442944.7:c.599T= ENSP00000392041.3:p.Leu200=
ENST00000536813.6:c.566T= ENSP00000438726.2:p.Leu189=
ENST00000546302.6:c.539T= ENSP00000445599.1:p.Leu180=
ENST00000640813.1:c.461+255T= ENSP00000491061.1:n.461+255T=
ENST00000648026.1:c.511T= ENSP00000498044.1:p.Cys171=
ENST00000648374.1:c.566T= ENSP00000497255.1:p.Leu189=
ENST00000648488.1:c.*90T= ENSP00000498079.1:n.*90T=
ENST00000649823.1:n.834T=
ENST00000650101.1:c.548T= ENSP00000496970.1:p.Leu183=
ENST00000650307.1:n.1443T=
ENST00000652429.1:c.617T= MANE Select ENSP00000498786.1:p.Leu206=
ENST00000278715.7:c.617T= ENSP00000278715.3:p.Leu206=
ENST00000392841.1:c.566T= ENSP00000376584.1:p.Leu189=
ENST00000442944.6:c.566T= ENSP00000392041.2:p.Leu189=
ENST00000537841.5:c.566T= ENSP00000444730.1:p.Leu189=
ENST00000542044.5:n.1062T=
ENST00000542345.5:n.755T=
ENST00000542729.5:c.566T= ENSP00000443058.1:p.Leu189=
ENST00000543090.5:c.559-275T= ENSP00000445429.1:n.559-275T=
ENST00000543543.5:n.852T=
ENST00000544182.1:n.592T=
ENST00000544387.5:c.617T= ENSP00000438424.1:p.Leu206=
ENST00000545621.5:c.*512T= ENSP00000444849.1:n.*512T=
ENST00000546226.5:n.905T=
ENST00000546302.5:c.539T= ENSP00000445599.1:p.Leu180=
NM_000190.3:c.617T= NP_000181.2:p.Leu206=
NM_001024382.1:c.566T= NP_001019553.1:p.Leu189=
NM_001258208.1:c.617T= NP_001245137.1:p.Leu206=
NM_001258209.1:c.566T= NP_001245138.1:p.Leu189=
XM_005271531.1:c.566T= XP_005271588.1:p.Leu189=
XM_005271532.1:c.566T= XP_005271589.1:p.Leu189=
XM_005271533.2:c.563T= XP_005271590.1:p.Leu188=
XM_011542796.1:c.452T= XP_011541098.1:p.Leu151=
NM_000190.4:c.617T= MANE Select NP_000181.2:p.Leu206=
NM_001024382.2:c.566T= NP_001019553.1:p.Leu189=
XM_005271533.3:c.563T= XP_005271590.1:p.Leu188=
XM_017017629.1:c.566T= XP_016873118.1:p.Leu189=
XM_024448460.1:c.563T= XP_024304228.1:p.Leu188=
NM_001258208.2:c.617T= NP_001245137.1:p.Leu206=
NM_001258209.2:c.566T= NP_001245138.1:p.Leu189=