Canonical Allele Identifier: CA382898743

Gene: HMBS

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119092958G>C , CM000673.2:g.119092958G>C	GRCh38
NC_000011.9:g.118963668G>C , CM000673.1:g.118963668G>C	GRCh37
NC_000011.8:g.118468878G>C	NCBI36
NG_008093.1:g.13082G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686218.1:c.684G>C	ENSP00000509288.1:p.Trp228Cys
ENST00000691144.1:n.3064G>C
ENST00000691249.1:n.1673G>C
ENST00000442944.7:c.831G>C	ENSP00000392041.3:p.Trp277Cys
ENST00000640813.1:c.*86G>C	ENSP00000491061.1:n.*86G>C
ENST00000648026.1:c.743G>C	ENSP00000498044.1:n.743G>C
ENST00000648374.1:c.798G>C	ENSP00000497255.1:p.Trp266Cys
ENST00000650101.1:c.780G>C	ENSP00000496970.1:p.Trp260Cys
ENST00000650307.1:n.1675G>C
ENST00000652429.1:c.849G>C MANE Select	ENSP00000498786.1:p.Trp283Cys
ENST00000278715.7:c.849G>C	ENSP00000278715.3:p.Trp283Cys
ENST00000392841.1:c.798G>C	ENSP00000376584.1:p.Trp266Cys
ENST00000442944.6:c.798G>C	ENSP00000392041.2:p.Trp266Cys
ENST00000537841.5:c.798G>C	ENSP00000444730.1:p.Trp266Cys
ENST00000539045.1:n.348G>C
ENST00000542044.5:n.1294G>C
ENST00000542729.5:c.678G>C	ENSP00000443058.1:p.Trp226Cys
ENST00000543090.5:c.756G>C	ENSP00000445429.1:p.Trp252Cys
ENST00000543543.5:n.1324G>C
ENST00000544182.1:n.1298G>C
ENST00000544387.5:c.729G>C	ENSP00000438424.1:p.Trp243Cys
ENST00000546226.5:n.1611G>C
NM_000190.3:c.849G>C	NP_000181.2:p.Trp283Cys
NM_001024382.1:c.798G>C	NP_001019553.1:p.Trp266Cys
NM_001258208.1:c.729G>C	NP_001245137.1:p.Trp243Cys
NM_001258209.1:c.678G>C	NP_001245138.1:p.Trp226Cys
XM_005271531.1:c.798G>C	XP_005271588.1:p.Trp266Cys
XM_005271532.1:c.798G>C	XP_005271589.1:p.Trp266Cys
XM_005271533.2:c.795G>C	XP_005271590.1:p.Trp265Cys
XM_011542796.1:c.684G>C	XP_011541098.1:p.Trp228Cys
NM_000190.4:c.849G>C MANE Select	NP_000181.2:p.Trp283Cys
NM_001024382.2:c.798G>C	NP_001019553.1:p.Trp266Cys
XM_005271533.3:c.795G>C	XP_005271590.1:p.Trp265Cys
XM_017017629.1:c.798G>C	XP_016873118.1:p.Trp266Cys
XM_024448460.1:c.675G>C	XP_024304228.1:p.Trp225Cys
NM_001258208.2:c.729G>C	NP_001245137.1:p.Trp243Cys
NM_001258209.2:c.678G>C	NP_001245138.1:p.Trp226Cys