Canonical Allele Identifier: CA382899668

Gene: HMBS

Linked Data

• MyVariant Identifiers: chr11:g.118963910G>T (hg19) ; chr11:g.119093200G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119093200G>T , CM000673.2:g.119093200G>T	GRCh38
NC_000011.9:g.118963910G>T , CM000673.1:g.118963910G>T	GRCh37
NC_000011.8:g.118469120G>T	NCBI36
NG_008093.1:g.13324G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686218.1:c.838G>T	ENSP00000509288.1:p.Gly280Cys
ENST00000691144.1:n.3218G>T
ENST00000691249.1:n.1827G>T
ENST00000442944.7:c.985G>T	ENSP00000392041.3:p.Gly329Cys
ENST00000640813.1:c.*240G>T	ENSP00000491061.1:n.*240G>T
ENST00000648026.1:c.897G>T	ENSP00000498044.1:n.897G>T
ENST00000648374.1:c.952G>T	ENSP00000497255.1:p.Gly318Cys
ENST00000650101.1:c.934G>T	ENSP00000496970.1:p.Gly312Cys
ENST00000650307.1:n.1829G>T
ENST00000652429.1:c.1003G>T MANE Select	ENSP00000498786.1:p.Gly335Cys
ENST00000278715.7:c.1003G>T	ENSP00000278715.3:p.Gly335Cys
ENST00000392841.1:c.952G>T	ENSP00000376584.1:p.Gly318Cys
ENST00000442944.6:c.952G>T	ENSP00000392041.2:p.Gly318Cys
ENST00000537841.5:c.952G>T	ENSP00000444730.1:p.Gly318Cys
ENST00000539045.1:n.502G>T
ENST00000542044.5:n.1448G>T
ENST00000542729.5:c.832G>T	ENSP00000443058.1:p.Gly278Cys
ENST00000543090.5:c.910G>T	ENSP00000445429.1:p.Gly304Cys
ENST00000543543.5:n.1478G>T
ENST00000544182.1:n.1452G>T
ENST00000544387.5:c.883G>T	ENSP00000438424.1:p.Gly295Cys
ENST00000546226.5:n.1765G>T
NM_000190.3:c.1003G>T	NP_000181.2:p.Gly335Cys
NM_001024382.1:c.952G>T	NP_001019553.1:p.Gly318Cys
NM_001258208.1:c.883G>T	NP_001245137.1:p.Gly295Cys
NM_001258209.1:c.832G>T	NP_001245138.1:p.Gly278Cys
XM_005271531.1:c.952G>T	XP_005271588.1:p.Gly318Cys
XM_005271532.1:c.952G>T	XP_005271589.1:p.Gly318Cys
XM_005271533.2:c.949G>T	XP_005271590.1:p.Gly317Cys
XM_011542796.1:c.838G>T	XP_011541098.1:p.Gly280Cys
NM_000190.4:c.1003G>T MANE Select	NP_000181.2:p.Gly335Cys
NM_001024382.2:c.952G>T	NP_001019553.1:p.Gly318Cys
XM_005271533.3:c.949G>T	XP_005271590.1:p.Gly317Cys
XM_017017629.1:c.952G>T	XP_016873118.1:p.Gly318Cys
XM_024448460.1:c.829G>T	XP_024304228.1:p.Gly277Cys
NM_001258208.2:c.883G>T	NP_001245137.1:p.Gly295Cys
NM_001258209.2:c.832G>T	NP_001245138.1:p.Gly278Cys