Canonical Allele Identifier: CA2003793430
Gene: HMBS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119093213C= , CM000673.2:g.119093213C= GRCh38
NC_000011.9:g.118963923C= , CM000673.1:g.118963923C= GRCh37
NC_000011.8:g.118469133C= NCBI36
NG_008093.1:g.13337C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000686218.1:c.851C= ENSP00000509288.1:p.Ala284=
ENST00000691144.1:n.3231C=
ENST00000691249.1:n.1840C=
ENST00000442944.7:c.998C= ENSP00000392041.3:p.Ala333=
ENST00000640813.1:c.*253C= ENSP00000491061.1:n.*253C=
ENST00000648026.1:c.910C= ENSP00000498044.1:n.910C=
ENST00000648374.1:c.965C= ENSP00000497255.1:p.Ala322=
ENST00000650101.1:c.947C= ENSP00000496970.1:p.Ala316=
ENST00000650307.1:n.1842C=
ENST00000652429.1:c.1016C= MANE Select ENSP00000498786.1:p.Ala339=
ENST00000278715.7:c.1016C= ENSP00000278715.3:p.Ala339=
ENST00000392841.1:c.965C= ENSP00000376584.1:p.Ala322=
ENST00000442944.6:c.965C= ENSP00000392041.2:p.Ala322=
ENST00000537841.5:c.965C= ENSP00000444730.1:p.Ala322=
ENST00000539045.1:n.515C=
ENST00000542044.5:n.1461C=
ENST00000542729.5:c.845C= ENSP00000443058.1:p.Ala282=
ENST00000543090.5:c.923C= ENSP00000445429.1:p.Ala308=
ENST00000543543.5:n.1491C=
ENST00000544182.1:n.1465C=
ENST00000544387.5:c.896C= ENSP00000438424.1:p.Ala299=
ENST00000546226.5:n.1778C=
NM_000190.3:c.1016C= NP_000181.2:p.Ala339=
NM_001024382.1:c.965C= NP_001019553.1:p.Ala322=
NM_001258208.1:c.896C= NP_001245137.1:p.Ala299=
NM_001258209.1:c.845C= NP_001245138.1:p.Ala282=
XM_005271531.1:c.965C= XP_005271588.1:p.Ala322=
XM_005271532.1:c.965C= XP_005271589.1:p.Ala322=
XM_005271533.2:c.962C= XP_005271590.1:p.Ala321=
XM_011542796.1:c.851C= XP_011541098.1:p.Ala284=
NM_000190.4:c.1016C= MANE Select NP_000181.2:p.Ala339=
NM_001024382.2:c.965C= NP_001019553.1:p.Ala322=
XM_005271533.3:c.962C= XP_005271590.1:p.Ala321=
XM_017017629.1:c.965C= XP_016873118.1:p.Ala322=
XM_024448460.1:c.842C= XP_024304228.1:p.Ala281=
NM_001258208.2:c.896C= NP_001245137.1:p.Ala299=
NM_001258209.2:c.845C= NP_001245138.1:p.Ala282=