Canonical Allele Identifier: CA477369261

Gene: HMBS

Linked Data

• MyVariant Identifiers: chr11:g.118963958C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119093248C>T , CM000673.2:g.119093248C>T	GRCh38
NC_000011.9:g.118963958C>T , CM000673.1:g.118963958C>T	GRCh37
NC_000011.8:g.118469168C>T	NCBI36
NG_008093.1:g.13372C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686218.1:c.886C>T	ENSP00000509288.1:p.Leu296=
ENST00000691144.1:n.3266C>T
ENST00000691249.1:n.1875C>T
ENST00000442944.7:c.1033C>T	ENSP00000392041.3:p.Leu345=
ENST00000640813.1:c.*288C>T	ENSP00000491061.1:n.*288C>T
ENST00000648026.1:c.945C>T	ENSP00000498044.1:n.945C>T
ENST00000648374.1:c.1000C>T	ENSP00000497255.1:p.Leu334=
ENST00000650101.1:c.982C>T	ENSP00000496970.1:p.Leu328=
ENST00000650307.1:n.1877C>T
ENST00000652429.1:c.1051C>T MANE Select	ENSP00000498786.1:p.Leu351=
ENST00000278715.7:c.1051C>T	ENSP00000278715.3:p.Leu351=
ENST00000392841.1:c.1000C>T	ENSP00000376584.1:p.Leu334=
ENST00000442944.6:c.1000C>T	ENSP00000392041.2:p.Leu334=
ENST00000537841.5:c.1000C>T	ENSP00000444730.1:p.Leu334=
ENST00000539045.1:n.550C>T
ENST00000542044.5:n.1496C>T
ENST00000542729.5:c.880C>T	ENSP00000443058.1:p.Leu294=
ENST00000543090.5:c.958C>T	ENSP00000445429.1:p.Leu320=
ENST00000543543.5:n.1526C>T
ENST00000544182.1:n.1500C>T
ENST00000544387.5:c.931C>T	ENSP00000438424.1:p.Leu311=
ENST00000546226.5:n.1813C>T
NM_000190.3:c.1051C>T	NP_000181.2:p.Leu351=
NM_001024382.1:c.1000C>T	NP_001019553.1:p.Leu334=
NM_001258208.1:c.931C>T	NP_001245137.1:p.Leu311=
NM_001258209.1:c.880C>T	NP_001245138.1:p.Leu294=
XM_005271531.1:c.1000C>T	XP_005271588.1:p.Leu334=
XM_005271532.1:c.1000C>T	XP_005271589.1:p.Leu334=
XM_005271533.2:c.997C>T	XP_005271590.1:p.Leu333=
XM_011542796.1:c.886C>T	XP_011541098.1:p.Leu296=
NM_000190.4:c.1051C>T MANE Select	NP_000181.2:p.Leu351=
NM_001024382.2:c.1000C>T	NP_001019553.1:p.Leu334=
XM_005271533.3:c.997C>T	XP_005271590.1:p.Leu333=
XM_017017629.1:c.1000C>T	XP_016873118.1:p.Leu334=
XM_024448460.1:c.877C>T	XP_024304228.1:p.Leu293=
NM_001258208.2:c.931C>T	NP_001245137.1:p.Leu311=
NM_001258209.2:c.880C>T	NP_001245138.1:p.Leu294=