Canonical Allele Identifier: CA477369254

Gene: HMBS

Linked Data

• MyVariant Identifiers: chr11:g.118963825A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119093115A>G , CM000673.2:g.119093115A>G	GRCh38
NC_000011.9:g.118963825A>G , CM000673.1:g.118963825A>G	GRCh37
NC_000011.8:g.118469035A>G	NCBI36
NG_008093.1:g.13239A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686218.1:c.753A>G	ENSP00000509288.1:p.Glu251=
ENST00000691144.1:n.3133A>G
ENST00000691249.1:n.1742A>G
ENST00000442944.7:c.900A>G	ENSP00000392041.3:p.Glu300=
ENST00000640813.1:c.*155A>G	ENSP00000491061.1:n.*155A>G
ENST00000648026.1:c.812A>G	ENSP00000498044.1:n.812A>G
ENST00000648374.1:c.867A>G	ENSP00000497255.1:p.Glu289=
ENST00000650101.1:c.849A>G	ENSP00000496970.1:p.Glu283=
ENST00000650307.1:n.1744A>G
ENST00000652429.1:c.918A>G MANE Select	ENSP00000498786.1:p.Glu306=
ENST00000278715.7:c.918A>G	ENSP00000278715.3:p.Glu306=
ENST00000392841.1:c.867A>G	ENSP00000376584.1:p.Glu289=
ENST00000442944.6:c.867A>G	ENSP00000392041.2:p.Glu289=
ENST00000537841.5:c.867A>G	ENSP00000444730.1:p.Glu289=
ENST00000539045.1:n.417A>G
ENST00000542044.5:n.1363A>G
ENST00000542729.5:c.747A>G	ENSP00000443058.1:p.Glu249=
ENST00000543090.5:c.825A>G	ENSP00000445429.1:p.Glu275=
ENST00000543543.5:n.1393A>G
ENST00000544182.1:n.1367A>G
ENST00000544387.5:c.798A>G	ENSP00000438424.1:p.Glu266=
ENST00000546226.5:n.1680A>G
NM_000190.3:c.918A>G	NP_000181.2:p.Glu306=
NM_001024382.1:c.867A>G	NP_001019553.1:p.Glu289=
NM_001258208.1:c.798A>G	NP_001245137.1:p.Glu266=
NM_001258209.1:c.747A>G	NP_001245138.1:p.Glu249=
XM_005271531.1:c.867A>G	XP_005271588.1:p.Glu289=
XM_005271532.1:c.867A>G	XP_005271589.1:p.Glu289=
XM_005271533.2:c.864A>G	XP_005271590.1:p.Glu288=
XM_011542796.1:c.753A>G	XP_011541098.1:p.Glu251=
NM_000190.4:c.918A>G MANE Select	NP_000181.2:p.Glu306=
NM_001024382.2:c.867A>G	NP_001019553.1:p.Glu289=
XM_005271533.3:c.864A>G	XP_005271590.1:p.Glu288=
XM_017017629.1:c.867A>G	XP_016873118.1:p.Glu289=
XM_024448460.1:c.744A>G	XP_024304228.1:p.Glu248=
NM_001258208.2:c.798A>G	NP_001245137.1:p.Glu266=
NM_001258209.2:c.747A>G	NP_001245138.1:p.Glu249=