Canonical Allele Identifier: CA2003791549
Gene: HMBS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119092430C= , CM000673.2:g.119092430C= GRCh38
NC_000011.9:g.118963140C= , CM000673.1:g.118963140C= GRCh37
NC_000011.8:g.118468350C= NCBI36
NG_008093.1:g.12554C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000686218.1:c.513C= ENSP00000509288.1:p.Ala171=
ENST00000691144.1:n.2659C=
ENST00000691249.1:n.1502C=
ENST00000442944.7:c.660C= ENSP00000392041.3:p.Ala220=
ENST00000536813.6:c.627C= ENSP00000438726.2:p.Ala209=
ENST00000640813.1:c.488C= ENSP00000491061.1:p.Pro163=
ENST00000648026.1:c.572C= ENSP00000498044.1:p.Pro191=
ENST00000648374.1:c.627C= ENSP00000497255.1:p.Ala209=
ENST00000649823.1:n.1135C=
ENST00000650101.1:c.609C= ENSP00000496970.1:p.Ala203=
ENST00000650307.1:n.1504C=
ENST00000652429.1:c.678C= MANE Select ENSP00000498786.1:p.Ala226=
ENST00000278715.7:c.678C= ENSP00000278715.3:p.Ala226=
ENST00000392841.1:c.627C= ENSP00000376584.1:p.Ala209=
ENST00000442944.6:c.627C= ENSP00000392041.2:p.Ala209=
ENST00000537841.5:c.627C= ENSP00000444730.1:p.Ala209=
ENST00000542044.5:n.1123C=
ENST00000542729.5:c.600+267C= ENSP00000443058.1:n.600+267C=
ENST00000543090.5:c.585C= ENSP00000445429.1:p.Ala195=
ENST00000543543.5:n.1153C=
ENST00000544182.1:n.893C=
ENST00000544387.5:c.651+267C= ENSP00000438424.1:n.651+267C=
ENST00000545621.5:c.*813C= ENSP00000444849.1:n.*813C=
ENST00000546226.5:n.1206C=
NM_000190.3:c.678C= NP_000181.2:p.Ala226=
NM_001024382.1:c.627C= NP_001019553.1:p.Ala209=
NM_001258208.1:c.651+267C= NP_001245137.1:n.651+267C=
NM_001258209.1:c.600+267C= NP_001245138.1:n.600+267C=
XM_005271531.1:c.627C= XP_005271588.1:p.Ala209=
XM_005271532.1:c.627C= XP_005271589.1:p.Ala209=
XM_005271533.2:c.624C= XP_005271590.1:p.Ala208=
XM_011542796.1:c.513C= XP_011541098.1:p.Ala171=
NM_000190.4:c.678C= MANE Select NP_000181.2:p.Ala226=
NM_001024382.2:c.627C= NP_001019553.1:p.Ala209=
XM_005271533.3:c.624C= XP_005271590.1:p.Ala208=
XM_017017629.1:c.627C= XP_016873118.1:p.Ala209=
XM_024448460.1:c.597+267C= XP_024304228.1:n.597+267C=
NM_001258208.2:c.651+267C= NP_001245137.1:n.651+267C=
NM_001258209.2:c.600+267C= NP_001245138.1:n.600+267C=