Canonical Allele Identifier: CA2003791561
Gene: HMBS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119092436C= , CM000673.2:g.119092436C= GRCh38
NC_000011.9:g.118963146C= , CM000673.1:g.118963146C= GRCh37
NC_000011.8:g.118468356C= NCBI36
NG_008093.1:g.12560C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000686218.1:c.519C= ENSP00000509288.1:p.Asp173=
ENST00000691144.1:n.2665C=
ENST00000691249.1:n.1508C=
ENST00000442944.7:c.666C= ENSP00000392041.3:p.Asp222=
ENST00000536813.6:c.633C= ENSP00000438726.2:p.Asp211=
ENST00000640813.1:c.494C= ENSP00000491061.1:p.Thr165=
ENST00000648026.1:c.578C= ENSP00000498044.1:p.Thr193=
ENST00000648374.1:c.633C= ENSP00000497255.1:p.Asp211=
ENST00000649823.1:n.1141C=
ENST00000650101.1:c.615C= ENSP00000496970.1:p.Asp205=
ENST00000650307.1:n.1510C=
ENST00000652429.1:c.684C= MANE Select ENSP00000498786.1:p.Asp228=
ENST00000278715.7:c.684C= ENSP00000278715.3:p.Asp228=
ENST00000392841.1:c.633C= ENSP00000376584.1:p.Asp211=
ENST00000442944.6:c.633C= ENSP00000392041.2:p.Asp211=
ENST00000537841.5:c.633C= ENSP00000444730.1:p.Asp211=
ENST00000542044.5:n.1129C=
ENST00000542729.5:c.600+273C= ENSP00000443058.1:n.600+273C=
ENST00000543090.5:c.591C= ENSP00000445429.1:p.Asp197=
ENST00000543543.5:n.1159C=
ENST00000544182.1:n.899C=
ENST00000544387.5:c.651+273C= ENSP00000438424.1:n.651+273C=
ENST00000545621.5:c.*819C= ENSP00000444849.1:n.*819C=
ENST00000546226.5:n.1212C=
NM_000190.3:c.684C= NP_000181.2:p.Asp228=
NM_001024382.1:c.633C= NP_001019553.1:p.Asp211=
NM_001258208.1:c.651+273C= NP_001245137.1:n.651+273C=
NM_001258209.1:c.600+273C= NP_001245138.1:n.600+273C=
XM_005271531.1:c.633C= XP_005271588.1:p.Asp211=
XM_005271532.1:c.633C= XP_005271589.1:p.Asp211=
XM_005271533.2:c.630C= XP_005271590.1:p.Asp210=
XM_011542796.1:c.519C= XP_011541098.1:p.Asp173=
NM_000190.4:c.684C= MANE Select NP_000181.2:p.Asp228=
NM_001024382.2:c.633C= NP_001019553.1:p.Asp211=
XM_005271533.3:c.630C= XP_005271590.1:p.Asp210=
XM_017017629.1:c.633C= XP_016873118.1:p.Asp211=
XM_024448460.1:c.597+273C= XP_024304228.1:n.597+273C=
NM_001258208.2:c.651+273C= NP_001245137.1:n.651+273C=
NM_001258209.2:c.600+273C= NP_001245138.1:n.600+273C=