Canonical Allele Identifier: CA2003791562
Gene: HMBS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119092438A= , CM000673.2:g.119092438A= GRCh38
NC_000011.9:g.118963148A= , CM000673.1:g.118963148A= GRCh37
NC_000011.8:g.118468358A= NCBI36
NG_008093.1:g.12562A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000686218.1:c.521A= ENSP00000509288.1:p.Gln174=
ENST00000691144.1:n.2667A=
ENST00000691249.1:n.1510A=
ENST00000442944.7:c.668A= ENSP00000392041.3:p.Gln223=
ENST00000536813.6:c.635A= ENSP00000438726.2:p.Gln212=
ENST00000640813.1:c.496A= ENSP00000491061.1:p.Arg166=
ENST00000648026.1:c.580A= ENSP00000498044.1:p.Arg194=
ENST00000648374.1:c.635A= ENSP00000497255.1:p.Gln212=
ENST00000649823.1:n.1143A=
ENST00000650101.1:c.617A= ENSP00000496970.1:p.Gln206=
ENST00000650307.1:n.1512A=
ENST00000652429.1:c.686A= MANE Select ENSP00000498786.1:p.Gln229=
ENST00000278715.7:c.686A= ENSP00000278715.3:p.Gln229=
ENST00000392841.1:c.635A= ENSP00000376584.1:p.Gln212=
ENST00000442944.6:c.635A= ENSP00000392041.2:p.Gln212=
ENST00000537841.5:c.635A= ENSP00000444730.1:p.Gln212=
ENST00000542044.5:n.1131A=
ENST00000542729.5:c.600+275A= ENSP00000443058.1:n.600+275A=
ENST00000543090.5:c.593A= ENSP00000445429.1:p.Gln198=
ENST00000543543.5:n.1161A=
ENST00000544182.1:n.901A=
ENST00000544387.5:c.651+275A= ENSP00000438424.1:n.651+275A=
ENST00000545621.5:c.*821A= ENSP00000444849.1:n.*821A=
ENST00000546226.5:n.1214A=
NM_000190.3:c.686A= NP_000181.2:p.Gln229=
NM_001024382.1:c.635A= NP_001019553.1:p.Gln212=
NM_001258208.1:c.651+275A= NP_001245137.1:n.651+275A=
NM_001258209.1:c.600+275A= NP_001245138.1:n.600+275A=
XM_005271531.1:c.635A= XP_005271588.1:p.Gln212=
XM_005271532.1:c.635A= XP_005271589.1:p.Gln212=
XM_005271533.2:c.632A= XP_005271590.1:p.Gln211=
XM_011542796.1:c.521A= XP_011541098.1:p.Gln174=
NM_000190.4:c.686A= MANE Select NP_000181.2:p.Gln229=
NM_001024382.2:c.635A= NP_001019553.1:p.Gln212=
XM_005271533.3:c.632A= XP_005271590.1:p.Gln211=
XM_017017629.1:c.635A= XP_016873118.1:p.Gln212=
XM_024448460.1:c.597+275A= XP_024304228.1:n.597+275A=
NM_001258208.2:c.651+275A= NP_001245137.1:n.651+275A=
NM_001258209.2:c.600+275A= NP_001245138.1:n.600+275A=