Canonical Allele Identifier: CA477128751

Gene: HMBS

Linked Data

• MyVariant Identifiers: chr11:g.118963209T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119092499T>G , CM000673.2:g.119092499T>G	GRCh38
NC_000011.9:g.118963209T>G , CM000673.1:g.118963209T>G	GRCh37
NC_000011.8:g.118468419T>G	NCBI36
NG_008093.1:g.12623T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686218.1:c.582T>G	ENSP00000509288.1:p.Ala194=
ENST00000691144.1:n.2728T>G
ENST00000691249.1:n.1571T>G
ENST00000442944.7:c.729T>G	ENSP00000392041.3:p.Ala243=
ENST00000640813.1:c.557T>G	ENSP00000491061.1:p.Leu186Arg
ENST00000648026.1:c.641T>G	ENSP00000498044.1:p.Leu214Arg
ENST00000648374.1:c.696T>G	ENSP00000497255.1:p.Ala232=
ENST00000649823.1:n.1204T>G
ENST00000650101.1:c.678T>G	ENSP00000496970.1:p.Ala226=
ENST00000650307.1:n.1573T>G
ENST00000652429.1:c.747T>G MANE Select	ENSP00000498786.1:p.Ala249=
ENST00000278715.7:c.747T>G	ENSP00000278715.3:p.Ala249=
ENST00000392841.1:c.696T>G	ENSP00000376584.1:p.Ala232=
ENST00000442944.6:c.696T>G	ENSP00000392041.2:p.Ala232=
ENST00000537841.5:c.696T>G	ENSP00000444730.1:p.Ala232=
ENST00000542044.5:n.1192T>G
ENST00000542729.5:c.601-259T>G	ENSP00000443058.1:n.601-259T>G
ENST00000543090.5:c.654T>G	ENSP00000445429.1:p.Ala218=
ENST00000543543.5:n.1222T>G
ENST00000544182.1:n.962T>G
ENST00000544387.5:c.652-259T>G	ENSP00000438424.1:n.652-259T>G
ENST00000545621.5:c.*882T>G	ENSP00000444849.1:n.*882T>G
ENST00000546226.5:n.1275T>G
NM_000190.3:c.747T>G	NP_000181.2:p.Ala249=
NM_001024382.1:c.696T>G	NP_001019553.1:p.Ala232=
NM_001258208.1:c.652-259T>G	NP_001245137.1:n.652-259T>G
NM_001258209.1:c.601-259T>G	NP_001245138.1:n.601-259T>G
XM_005271531.1:c.696T>G	XP_005271588.1:p.Ala232=
XM_005271532.1:c.696T>G	XP_005271589.1:p.Ala232=
XM_005271533.2:c.693T>G	XP_005271590.1:p.Ala231=
XM_011542796.1:c.582T>G	XP_011541098.1:p.Ala194=
NM_000190.4:c.747T>G MANE Select	NP_000181.2:p.Ala249=
NM_001024382.2:c.696T>G	NP_001019553.1:p.Ala232=
XM_005271533.3:c.693T>G	XP_005271590.1:p.Ala231=
XM_017017629.1:c.696T>G	XP_016873118.1:p.Ala232=
XM_024448460.1:c.598-259T>G	XP_024304228.1:n.598-259T>G
NM_001258208.2:c.652-259T>G	NP_001245137.1:n.652-259T>G
NM_001258209.2:c.601-259T>G	NP_001245138.1:n.601-259T>G