Canonical Allele Identifier: CA2003793340

Gene: HMBS

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119093167C= , CM000673.2:g.119093167C=	GRCh38
NC_000011.9:g.118963877C= , CM000673.1:g.118963877C=	GRCh37
NC_000011.8:g.118469087C=	NCBI36
NG_008093.1:g.13291C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686218.1:c.805C=	ENSP00000509288.1:p.Pro269=
ENST00000691144.1:n.3185C=
ENST00000691249.1:n.1794C=
ENST00000442944.7:c.952C=	ENSP00000392041.3:p.Pro318=
ENST00000640813.1:c.*207C=	ENSP00000491061.1:n.*207C=
ENST00000648026.1:c.864C=	ENSP00000498044.1:n.864C=
ENST00000648374.1:c.919C=	ENSP00000497255.1:p.Pro307=
ENST00000650101.1:c.901C=	ENSP00000496970.1:p.Pro301=
ENST00000650307.1:n.1796C=
ENST00000652429.1:c.970C= MANE Select	ENSP00000498786.1:p.Pro324=
ENST00000278715.7:c.970C=	ENSP00000278715.3:p.Pro324=
ENST00000392841.1:c.919C=	ENSP00000376584.1:p.Pro307=
ENST00000442944.6:c.919C=	ENSP00000392041.2:p.Pro307=
ENST00000537841.5:c.919C=	ENSP00000444730.1:p.Pro307=
ENST00000539045.1:n.469C=
ENST00000542044.5:n.1415C=
ENST00000542729.5:c.799C=	ENSP00000443058.1:p.Pro267=
ENST00000543090.5:c.877C=	ENSP00000445429.1:p.Pro293=
ENST00000543543.5:n.1445C=
ENST00000544182.1:n.1419C=
ENST00000544387.5:c.850C=	ENSP00000438424.1:p.Pro284=
ENST00000546226.5:n.1732C=
NM_000190.3:c.970C=	NP_000181.2:p.Pro324=
NM_001024382.1:c.919C=	NP_001019553.1:p.Pro307=
NM_001258208.1:c.850C=	NP_001245137.1:p.Pro284=
NM_001258209.1:c.799C=	NP_001245138.1:p.Pro267=
XM_005271531.1:c.919C=	XP_005271588.1:p.Pro307=
XM_005271532.1:c.919C=	XP_005271589.1:p.Pro307=
XM_005271533.2:c.916C=	XP_005271590.1:p.Pro306=
XM_011542796.1:c.805C=	XP_011541098.1:p.Pro269=
NM_000190.4:c.970C= MANE Select	NP_000181.2:p.Pro324=
NM_001024382.2:c.919C=	NP_001019553.1:p.Pro307=
XM_005271533.3:c.916C=	XP_005271590.1:p.Pro306=
XM_017017629.1:c.919C=	XP_016873118.1:p.Pro307=
XM_024448460.1:c.796C=	XP_024304228.1:p.Pro266=
NM_001258208.2:c.850C=	NP_001245137.1:p.Pro284=
NM_001258209.2:c.799C=	NP_001245138.1:p.Pro267=