Canonical Allele Identifier: CA2003793256
Gene: HMBS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119093134C= , CM000673.2:g.119093134C= GRCh38
NC_000011.9:g.118963844C= , CM000673.1:g.118963844C= GRCh37
NC_000011.8:g.118469054C= NCBI36
NG_008093.1:g.13258C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000686218.1:c.772C= ENSP00000509288.1:p.Pro258=
ENST00000691144.1:n.3152C=
ENST00000691249.1:n.1761C=
ENST00000442944.7:c.919C= ENSP00000392041.3:p.Pro307=
ENST00000640813.1:c.*174C= ENSP00000491061.1:n.*174C=
ENST00000648026.1:c.831C= ENSP00000498044.1:n.831C=
ENST00000648374.1:c.886C= ENSP00000497255.1:p.Pro296=
ENST00000650101.1:c.868C= ENSP00000496970.1:p.Pro290=
ENST00000650307.1:n.1763C=
ENST00000652429.1:c.937C= MANE Select ENSP00000498786.1:p.Pro313=
ENST00000278715.7:c.937C= ENSP00000278715.3:p.Pro313=
ENST00000392841.1:c.886C= ENSP00000376584.1:p.Pro296=
ENST00000442944.6:c.886C= ENSP00000392041.2:p.Pro296=
ENST00000537841.5:c.886C= ENSP00000444730.1:p.Pro296=
ENST00000539045.1:n.436C=
ENST00000542044.5:n.1382C=
ENST00000542729.5:c.766C= ENSP00000443058.1:p.Pro256=
ENST00000543090.5:c.844C= ENSP00000445429.1:p.Pro282=
ENST00000543543.5:n.1412C=
ENST00000544182.1:n.1386C=
ENST00000544387.5:c.817C= ENSP00000438424.1:p.Pro273=
ENST00000546226.5:n.1699C=
NM_000190.3:c.937C= NP_000181.2:p.Pro313=
NM_001024382.1:c.886C= NP_001019553.1:p.Pro296=
NM_001258208.1:c.817C= NP_001245137.1:p.Pro273=
NM_001258209.1:c.766C= NP_001245138.1:p.Pro256=
XM_005271531.1:c.886C= XP_005271588.1:p.Pro296=
XM_005271532.1:c.886C= XP_005271589.1:p.Pro296=
XM_005271533.2:c.883C= XP_005271590.1:p.Pro295=
XM_011542796.1:c.772C= XP_011541098.1:p.Pro258=
NM_000190.4:c.937C= MANE Select NP_000181.2:p.Pro313=
NM_001024382.2:c.886C= NP_001019553.1:p.Pro296=
XM_005271533.3:c.883C= XP_005271590.1:p.Pro295=
XM_017017629.1:c.886C= XP_016873118.1:p.Pro296=
XM_024448460.1:c.763C= XP_024304228.1:p.Pro255=
NM_001258208.2:c.817C= NP_001245137.1:p.Pro273=
NM_001258209.2:c.766C= NP_001245138.1:p.Pro256=