Canonical Allele Identifier: CA2003791484

Gene: HMBS

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119092416G= , CM000673.2:g.119092416G=	GRCh38
NC_000011.9:g.118963126G= , CM000673.1:g.118963126G=	GRCh37
NC_000011.8:g.118468336G=	NCBI36
NG_008093.1:g.12540G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000686218.1:c.499G=	ENSP00000509288.1:p.Val167=
ENST00000691144.1:n.2645G=
ENST00000691249.1:n.1488G=
ENST00000442944.7:c.646G=	ENSP00000392041.3:p.Val216=
ENST00000536813.6:c.613G=	ENSP00000438726.2:p.Val205=
ENST00000640813.1:c.474G=	ENSP00000491061.1:p.Ala158=
ENST00000648026.1:c.558G=	ENSP00000498044.1:p.Ala186=
ENST00000648374.1:c.613G=	ENSP00000497255.1:p.Val205=
ENST00000649823.1:n.1121G=
ENST00000650101.1:c.595G=	ENSP00000496970.1:p.Val199=
ENST00000650307.1:n.1490G=
ENST00000652429.1:c.664G= MANE Select	ENSP00000498786.1:p.Val222=
ENST00000278715.7:c.664G=	ENSP00000278715.3:p.Val222=
ENST00000392841.1:c.613G=	ENSP00000376584.1:p.Val205=
ENST00000442944.6:c.613G=	ENSP00000392041.2:p.Val205=
ENST00000537841.5:c.613G=	ENSP00000444730.1:p.Val205=
ENST00000542044.5:n.1109G=
ENST00000542729.5:c.600+253G=	ENSP00000443058.1:n.600+253G=
ENST00000543090.5:c.571G=	ENSP00000445429.1:p.Val191=
ENST00000543543.5:n.1139G=
ENST00000544182.1:n.879G=
ENST00000544387.5:c.651+253G=	ENSP00000438424.1:n.651+253G=
ENST00000545621.5:c.*799G=	ENSP00000444849.1:n.*799G=
ENST00000546226.5:n.1192G=
NM_000190.3:c.664G=	NP_000181.2:p.Val222=
NM_001024382.1:c.613G=	NP_001019553.1:p.Val205=
NM_001258208.1:c.651+253G=	NP_001245137.1:n.651+253G=
NM_001258209.1:c.600+253G=	NP_001245138.1:n.600+253G=
XM_005271531.1:c.613G=	XP_005271588.1:p.Val205=
XM_005271532.1:c.613G=	XP_005271589.1:p.Val205=
XM_005271533.2:c.610G=	XP_005271590.1:p.Val204=
XM_011542796.1:c.499G=	XP_011541098.1:p.Val167=
NM_000190.4:c.664G= MANE Select	NP_000181.2:p.Val222=
NM_001024382.2:c.613G=	NP_001019553.1:p.Val205=
XM_005271533.3:c.610G=	XP_005271590.1:p.Val204=
XM_017017629.1:c.613G=	XP_016873118.1:p.Val205=
XM_024448460.1:c.597+253G=	XP_024304228.1:n.597+253G=
NM_001258208.2:c.651+253G=	NP_001245137.1:n.651+253G=
NM_001258209.2:c.600+253G=	NP_001245138.1:n.600+253G=