Canonical Allele Identifier: CA477369292

Gene: HMBS

Linked Data

• MyVariant Identifiers: chr11:g.118963864T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119093154T>A , CM000673.2:g.119093154T>A	GRCh38
NC_000011.9:g.118963864T>A , CM000673.1:g.118963864T>A	GRCh37
NC_000011.8:g.118469074T>A	NCBI36
NG_008093.1:g.13278T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686218.1:c.792T>A	ENSP00000509288.1:p.Thr264=
ENST00000691144.1:n.3172T>A
ENST00000691249.1:n.1781T>A
ENST00000442944.7:c.939T>A	ENSP00000392041.3:p.Thr313=
ENST00000640813.1:c.*194T>A	ENSP00000491061.1:n.*194T>A
ENST00000648026.1:c.851T>A	ENSP00000498044.1:n.851T>A
ENST00000648374.1:c.906T>A	ENSP00000497255.1:p.Thr302=
ENST00000650101.1:c.888T>A	ENSP00000496970.1:p.Thr296=
ENST00000650307.1:n.1783T>A
ENST00000652429.1:c.957T>A MANE Select	ENSP00000498786.1:p.Thr319=
ENST00000278715.7:c.957T>A	ENSP00000278715.3:p.Thr319=
ENST00000392841.1:c.906T>A	ENSP00000376584.1:p.Thr302=
ENST00000442944.6:c.906T>A	ENSP00000392041.2:p.Thr302=
ENST00000537841.5:c.906T>A	ENSP00000444730.1:p.Thr302=
ENST00000539045.1:n.456T>A
ENST00000542044.5:n.1402T>A
ENST00000542729.5:c.786T>A	ENSP00000443058.1:p.Thr262=
ENST00000543090.5:c.864T>A	ENSP00000445429.1:p.Thr288=
ENST00000543543.5:n.1432T>A
ENST00000544182.1:n.1406T>A
ENST00000544387.5:c.837T>A	ENSP00000438424.1:p.Thr279=
ENST00000546226.5:n.1719T>A
NM_000190.3:c.957T>A	NP_000181.2:p.Thr319=
NM_001024382.1:c.906T>A	NP_001019553.1:p.Thr302=
NM_001258208.1:c.837T>A	NP_001245137.1:p.Thr279=
NM_001258209.1:c.786T>A	NP_001245138.1:p.Thr262=
XM_005271531.1:c.906T>A	XP_005271588.1:p.Thr302=
XM_005271532.1:c.906T>A	XP_005271589.1:p.Thr302=
XM_005271533.2:c.903T>A	XP_005271590.1:p.Thr301=
XM_011542796.1:c.792T>A	XP_011541098.1:p.Thr264=
NM_000190.4:c.957T>A MANE Select	NP_000181.2:p.Thr319=
NM_001024382.2:c.906T>A	NP_001019553.1:p.Thr302=
XM_005271533.3:c.903T>A	XP_005271590.1:p.Thr301=
XM_017017629.1:c.906T>A	XP_016873118.1:p.Thr302=
XM_024448460.1:c.783T>A	XP_024304228.1:p.Thr261=
NM_001258208.2:c.837T>A	NP_001245137.1:p.Thr279=
NM_001258209.2:c.786T>A	NP_001245138.1:p.Thr262=