Canonical Allele Identifier: CA2003782595

Gene: HMBS

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119089284T= , CM000673.2:g.119089284T=	GRCh38
NC_000011.9:g.118959994T= , CM000673.1:g.118959994T=	GRCh37
NC_000011.8:g.118465204T=	NCBI36
NG_008093.1:g.9408T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686218.1:c.101+12T=	ENSP00000509288.1:n.101+12T=
ENST00000686690.1:n.887+12T=
ENST00000691144.1:n.2007+12T=
ENST00000691249.1:n.850+12T=
ENST00000442944.7:c.248+12T=	ENSP00000392041.3:n.248+12T=
ENST00000534956.2:n.215+12T=
ENST00000536813.6:c.215+12T=	ENSP00000438726.2:n.215+12T=
ENST00000546302.6:c.266+12T=	ENSP00000445599.1:n.266+12T=
ENST00000640813.1:c.215+12T=	ENSP00000491061.1:n.215+12T=
ENST00000648026.1:c.260+12T=	ENSP00000498044.1:n.260+12T=
ENST00000648374.1:c.215+12T=	ENSP00000497255.1:n.215+12T=
ENST00000648488.1:c.215+12T=	ENSP00000498079.1:n.215+12T=
ENST00000649823.1:n.483+12T=
ENST00000649868.1:c.121+12T=	ENSP00000497548.1:n.121+12T=
ENST00000650101.1:c.197+12T=	ENSP00000496970.1:n.197+12T=
ENST00000650307.1:n.1092+12T=
ENST00000652429.1:c.266+12T= MANE Select	ENSP00000498786.1:n.266+12T=
ENST00000278715.7:c.266+12T=	ENSP00000278715.3:n.266+12T=
ENST00000392841.1:c.215+12T=	ENSP00000376584.1:n.215+12T=
ENST00000442944.6:c.215+12T=	ENSP00000392041.2:n.215+12T=
ENST00000534956.1:n.182+12T=
ENST00000535253.5:c.215+12T=	ENSP00000442079.1:n.215+12T=
ENST00000535793.5:c.*161+12T=	ENSP00000439904.1:n.*161+12T=
ENST00000536185.5:n.384+12T=
ENST00000536813.5:c.248+12T=	ENSP00000438726.1:n.248+12T=
ENST00000537841.5:c.215+12T=	ENSP00000444730.1:n.215+12T=
ENST00000539986.5:c.215+12T=	ENSP00000440092.1:n.215+12T=
ENST00000542044.5:n.711+12T=
ENST00000542345.5:n.404+12T=
ENST00000542729.5:c.215+12T=	ENSP00000443058.1:n.215+12T=
ENST00000542822.5:c.*202+12T=	ENSP00000444817.1:n.*202+12T=
ENST00000543090.5:c.212+12T=	ENSP00000445429.1:n.212+12T=
ENST00000543543.5:n.501+12T=
ENST00000543821.5:n.412+12T=
ENST00000544360.5:n.234+12T=
ENST00000544387.5:c.266+12T=	ENSP00000438424.1:n.266+12T=
ENST00000545621.5:c.*161+12T=	ENSP00000444849.1:n.*161+12T=
ENST00000546226.5:n.325+12T=
ENST00000546302.5:c.266+12T=	ENSP00000445599.1:n.266+12T=
NM_000190.3:c.266+12T=	NP_000181.2:n.266+12T=
NM_001024382.1:c.215+12T=	NP_001019553.1:n.215+12T=
NM_001258208.1:c.266+12T=	NP_001245137.1:n.266+12T=
NM_001258209.1:c.215+12T=	NP_001245138.1:n.215+12T=
XM_005271531.1:c.215+12T=	XP_005271588.1:n.215+12T=
XM_005271532.1:c.215+12T=	XP_005271589.1:n.215+12T=
XM_005271533.2:c.212+12T=	XP_005271590.1:n.212+12T=
XM_011542796.1:c.101+12T=	XP_011541098.1:n.101+12T=
NM_000190.4:c.266+12T= MANE Select	NP_000181.2:n.266+12T=
NM_001024382.2:c.215+12T=	NP_001019553.1:n.215+12T=
XM_005271533.3:c.212+12T=	XP_005271590.1:n.212+12T=
XM_017017629.1:c.215+12T=	XP_016873118.1:n.215+12T=
XM_024448460.1:c.212+12T=	XP_024304228.1:n.212+12T=
NM_001258208.2:c.266+12T=	NP_001245137.1:n.266+12T=
NM_001258209.2:c.215+12T=	NP_001245138.1:n.215+12T=