Canonical Allele Identifier: CA2003783653
Gene: HMBS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119091507G= , CM000673.2:g.119091507G= GRCh38
NC_000011.9:g.118962217G= , CM000673.1:g.118962217G= GRCh37
NC_000011.8:g.118467427G= NCBI36
NG_008093.1:g.11631G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000686218.1:c.428G= ENSP00000509288.1:p.Trp143=
ENST00000686690.1:n.1443G=
ENST00000691144.1:n.2334G=
ENST00000691249.1:n.1177G=
ENST00000442944.7:c.575G= ENSP00000392041.3:p.Trp192=
ENST00000534956.2:n.448-354G=
ENST00000536813.6:c.542G= ENSP00000438726.2:p.Trp181=
ENST00000546302.6:c.515G= ENSP00000445599.1:p.Trp172=
ENST00000640813.1:c.448-354G= ENSP00000491061.1:n.448-354G=
ENST00000648026.1:c.493-354G= ENSP00000498044.1:n.493-354G=
ENST00000648374.1:c.542G= ENSP00000497255.1:p.Trp181=
ENST00000648488.1:c.*85+251G= ENSP00000498079.1:n.*85+251G=
ENST00000649823.1:n.810G=
ENST00000649868.1:c.*207-354G= ENSP00000497548.1:n.*207-354G=
ENST00000650101.1:c.524G= ENSP00000496970.1:p.Trp175=
ENST00000650307.1:n.1419G=
ENST00000652429.1:c.593G= MANE Select ENSP00000498786.1:p.Trp198=
ENST00000278715.7:c.593G= ENSP00000278715.3:p.Trp198=
ENST00000392841.1:c.542G= ENSP00000376584.1:p.Trp181=
ENST00000442944.6:c.542G= ENSP00000392041.2:p.Trp181=
ENST00000534956.1:n.415-354G=
ENST00000535253.5:c.542G= ENSP00000442079.1:p.Trp181=
ENST00000535793.5:c.*488G= ENSP00000439904.1:n.*488G=
ENST00000537841.5:c.542G= ENSP00000444730.1:p.Trp181=
ENST00000539986.5:c.542G= ENSP00000440092.1:p.Trp181=
ENST00000542044.5:n.1038G=
ENST00000542345.5:n.731G=
ENST00000542729.5:c.542G= ENSP00000443058.1:p.Trp181=
ENST00000542822.5:c.*529G= ENSP00000444817.1:n.*529G=
ENST00000543090.5:c.539G= ENSP00000445429.1:p.Trp180=
ENST00000543543.5:n.828G=
ENST00000544360.5:n.561G=
ENST00000544387.5:c.593G= ENSP00000438424.1:p.Trp198=
ENST00000545621.5:c.*488G= ENSP00000444849.1:n.*488G=
ENST00000546226.5:n.881G=
ENST00000546302.5:c.515G= ENSP00000445599.1:p.Trp172=
NM_000190.3:c.593G= NP_000181.2:p.Trp198=
NM_001024382.1:c.542G= NP_001019553.1:p.Trp181=
NM_001258208.1:c.593G= NP_001245137.1:p.Trp198=
NM_001258209.1:c.542G= NP_001245138.1:p.Trp181=
XM_005271531.1:c.542G= XP_005271588.1:p.Trp181=
XM_005271532.1:c.542G= XP_005271589.1:p.Trp181=
XM_005271533.2:c.539G= XP_005271590.1:p.Trp180=
XM_011542796.1:c.428G= XP_011541098.1:p.Trp143=
NM_000190.4:c.593G= MANE Select NP_000181.2:p.Trp198=
NM_001024382.2:c.542G= NP_001019553.1:p.Trp181=
XM_005271533.3:c.539G= XP_005271590.1:p.Trp180=
XM_017017629.1:c.542G= XP_016873118.1:p.Trp181=
XM_024448460.1:c.539G= XP_024304228.1:p.Trp180=
NM_001258208.2:c.593G= NP_001245137.1:p.Trp198=
NM_001258209.2:c.542G= NP_001245138.1:p.Trp181=