Canonical Allele Identifier: CA382892727

Gene: HMBS

Linked Data

• MyVariant Identifiers: chr11:g.118960762C>T (hg19) ; chr11:g.119090052C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119090052C>T , CM000673.2:g.119090052C>T	GRCh38
NC_000011.9:g.118960762C>T , CM000673.1:g.118960762C>T	GRCh37
NC_000011.8:g.118465972C>T	NCBI36
NG_008093.1:g.10176C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000686218.1:c.242C>T	ENSP00000509288.1:p.Thr81Ile
ENST00000686690.1:n.1257C>T
ENST00000691144.1:n.2148C>T
ENST00000691249.1:n.991C>T
ENST00000442944.7:c.389C>T	ENSP00000392041.3:p.Thr130Ile
ENST00000534956.2:n.356C>T
ENST00000536813.6:c.356C>T	ENSP00000438726.2:p.Thr119Ile
ENST00000546302.6:c.329C>T	ENSP00000445599.1:p.Thr110Ile
ENST00000640813.1:c.356C>T	ENSP00000491061.1:p.Thr119Ile
ENST00000648026.1:c.401C>T	ENSP00000498044.1:p.Thr134Ile
ENST00000648374.1:c.356C>T	ENSP00000497255.1:p.Thr119Ile
ENST00000648488.1:c.356C>T	ENSP00000498079.1:p.Thr119Ile
ENST00000649823.1:n.624C>T
ENST00000649868.1:c.*115C>T	ENSP00000497548.1:n.*115C>T
ENST00000650101.1:c.338C>T	ENSP00000496970.1:p.Thr113Ile
ENST00000650307.1:n.1233C>T
ENST00000652429.1:c.407C>T MANE Select	ENSP00000498786.1:p.Thr136Ile
ENST00000278715.7:c.407C>T	ENSP00000278715.3:p.Thr136Ile
ENST00000392841.1:c.356C>T	ENSP00000376584.1:p.Thr119Ile
ENST00000442944.6:c.356C>T	ENSP00000392041.2:p.Thr119Ile
ENST00000534956.1:n.323C>T
ENST00000535253.5:c.356C>T	ENSP00000442079.1:p.Thr119Ile
ENST00000535793.5:c.*302C>T	ENSP00000439904.1:n.*302C>T
ENST00000537841.5:c.356C>T	ENSP00000444730.1:p.Thr119Ile
ENST00000539986.5:c.356C>T	ENSP00000440092.1:p.Thr119Ile
ENST00000542044.5:n.852C>T
ENST00000542345.5:n.545C>T
ENST00000542729.5:c.356C>T	ENSP00000443058.1:p.Thr119Ile
ENST00000542822.5:c.*343C>T	ENSP00000444817.1:n.*343C>T
ENST00000543090.5:c.353C>T	ENSP00000445429.1:p.Thr118Ile
ENST00000543543.5:n.642C>T
ENST00000544360.5:n.375C>T
ENST00000544387.5:c.407C>T	ENSP00000438424.1:p.Thr136Ile
ENST00000545621.5:c.*302C>T	ENSP00000444849.1:n.*302C>T
ENST00000546226.5:n.695C>T
ENST00000546302.5:c.329C>T	ENSP00000445599.1:p.Thr110Ile
NM_000190.3:c.407C>T	NP_000181.2:p.Thr136Ile
NM_001024382.1:c.356C>T	NP_001019553.1:p.Thr119Ile
NM_001258208.1:c.407C>T	NP_001245137.1:p.Thr136Ile
NM_001258209.1:c.356C>T	NP_001245138.1:p.Thr119Ile
XM_005271531.1:c.356C>T	XP_005271588.1:p.Thr119Ile
XM_005271532.1:c.356C>T	XP_005271589.1:p.Thr119Ile
XM_005271533.2:c.353C>T	XP_005271590.1:p.Thr118Ile
XM_011542796.1:c.242C>T	XP_011541098.1:p.Thr81Ile
NM_000190.4:c.407C>T MANE Select	NP_000181.2:p.Thr136Ile
NM_001024382.2:c.356C>T	NP_001019553.1:p.Thr119Ile
XM_005271533.3:c.353C>T	XP_005271590.1:p.Thr118Ile
XM_017017629.1:c.356C>T	XP_016873118.1:p.Thr119Ile
XM_024448460.1:c.353C>T	XP_024304228.1:p.Thr118Ile
NM_001258208.2:c.407C>T	NP_001245137.1:p.Thr136Ile
NM_001258209.2:c.356C>T	NP_001245138.1:p.Thr119Ile