Canonical Allele Identifier: CA477124982

Gene: HMBS

Linked Data

• MyVariant Identifiers: chr11:g.118960408T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119089698T>A , CM000673.2:g.119089698T>A	GRCh38
NC_000011.9:g.118960408T>A , CM000673.1:g.118960408T>A	GRCh37
NC_000011.8:g.118465618T>A	NCBI36
NG_008093.1:g.9822T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686218.1:c.117T>A	ENSP00000509288.1:p.Val39=
ENST00000686690.1:n.903T>A
ENST00000691144.1:n.2023T>A
ENST00000691249.1:n.866T>A
ENST00000442944.7:c.264T>A	ENSP00000392041.3:p.Val88=
ENST00000534956.2:n.231T>A
ENST00000536813.6:c.231T>A	ENSP00000438726.2:p.Val77=
ENST00000546302.6:c.267-292T>A	ENSP00000445599.1:n.267-292T>A
ENST00000640813.1:c.231T>A	ENSP00000491061.1:p.Val77=
ENST00000648026.1:c.276T>A	ENSP00000498044.1:p.Val92=
ENST00000648374.1:c.231T>A	ENSP00000497255.1:p.Val77=
ENST00000648488.1:c.231T>A	ENSP00000498079.1:p.Val77=
ENST00000649823.1:n.499T>A
ENST00000649868.1:c.137T>A	ENSP00000497548.1:p.Phe46Tyr
ENST00000650101.1:c.213T>A	ENSP00000496970.1:p.Val71=
ENST00000650307.1:n.1108T>A
ENST00000652429.1:c.282T>A MANE Select	ENSP00000498786.1:p.Val94=
ENST00000278715.7:c.282T>A	ENSP00000278715.3:p.Val94=
ENST00000392841.1:c.231T>A	ENSP00000376584.1:p.Val77=
ENST00000442944.6:c.231T>A	ENSP00000392041.2:p.Val77=
ENST00000534956.1:n.198T>A
ENST00000535253.5:c.231T>A	ENSP00000442079.1:p.Val77=
ENST00000535793.5:c.*177T>A	ENSP00000439904.1:n.*177T>A
ENST00000536185.5:n.400T>A
ENST00000536813.5:c.264T>A	ENSP00000438726.1:p.Val88=
ENST00000537841.5:c.231T>A	ENSP00000444730.1:p.Val77=
ENST00000539986.5:c.231T>A	ENSP00000440092.1:p.Val77=
ENST00000542044.5:n.727T>A
ENST00000542345.5:n.420T>A
ENST00000542729.5:c.231T>A	ENSP00000443058.1:p.Val77=
ENST00000542822.5:c.*218T>A	ENSP00000444817.1:n.*218T>A
ENST00000543090.5:c.228T>A	ENSP00000445429.1:p.Val76=
ENST00000543543.5:n.517T>A
ENST00000543821.5:n.428T>A
ENST00000544360.5:n.250T>A
ENST00000544387.5:c.282T>A	ENSP00000438424.1:p.Val94=
ENST00000545621.5:c.*177T>A	ENSP00000444849.1:n.*177T>A
ENST00000546226.5:n.341T>A
ENST00000546302.5:c.267-292T>A	ENSP00000445599.1:n.267-292T>A
NM_000190.3:c.282T>A	NP_000181.2:p.Val94=
NM_001024382.1:c.231T>A	NP_001019553.1:p.Val77=
NM_001258208.1:c.282T>A	NP_001245137.1:p.Val94=
NM_001258209.1:c.231T>A	NP_001245138.1:p.Val77=
XM_005271531.1:c.231T>A	XP_005271588.1:p.Val77=
XM_005271532.1:c.231T>A	XP_005271589.1:p.Val77=
XM_005271533.2:c.228T>A	XP_005271590.1:p.Val76=
XM_011542796.1:c.117T>A	XP_011541098.1:p.Val39=
NM_000190.4:c.282T>A MANE Select	NP_000181.2:p.Val94=
NM_001024382.2:c.231T>A	NP_001019553.1:p.Val77=
XM_005271533.3:c.228T>A	XP_005271590.1:p.Val76=
XM_017017629.1:c.231T>A	XP_016873118.1:p.Val77=
XM_024448460.1:c.228T>A	XP_024304228.1:p.Val76=
NM_001258208.2:c.282T>A	NP_001245137.1:p.Val94=
NM_001258209.2:c.231T>A	NP_001245138.1:p.Val77=