Canonical Allele Identifier: CA382897517

Gene: HMBS

Linked Data

• MyVariant Identifiers: chr11:g.118963161T>G (hg19) ; chr11:g.119092451T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119092451T>G , CM000673.2:g.119092451T>G	GRCh38
NC_000011.9:g.118963161T>G , CM000673.1:g.118963161T>G	GRCh37
NC_000011.8:g.118468371T>G	NCBI36
NG_008093.1:g.12575T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686218.1:c.534T>G	ENSP00000509288.1:p.Asp178Glu
ENST00000691144.1:n.2680T>G
ENST00000691249.1:n.1523T>G
ENST00000442944.7:c.681T>G	ENSP00000392041.3:p.Asp227Glu
ENST00000536813.6:c.648T>G	ENSP00000438726.2:p.Asp216Glu
ENST00000640813.1:c.509T>G	ENSP00000491061.1:p.Ile170Ser
ENST00000648026.1:c.593T>G	ENSP00000498044.1:p.Ile198Ser
ENST00000648374.1:c.648T>G	ENSP00000497255.1:p.Asp216Glu
ENST00000649823.1:n.1156T>G
ENST00000650101.1:c.630T>G	ENSP00000496970.1:p.Asp210Glu
ENST00000650307.1:n.1525T>G
ENST00000652429.1:c.699T>G MANE Select	ENSP00000498786.1:p.Asp233Glu
ENST00000278715.7:c.699T>G	ENSP00000278715.3:p.Asp233Glu
ENST00000392841.1:c.648T>G	ENSP00000376584.1:p.Asp216Glu
ENST00000442944.6:c.648T>G	ENSP00000392041.2:p.Asp216Glu
ENST00000537841.5:c.648T>G	ENSP00000444730.1:p.Asp216Glu
ENST00000542044.5:n.1144T>G
ENST00000542729.5:c.600+288T>G	ENSP00000443058.1:n.600+288T>G
ENST00000543090.5:c.606T>G	ENSP00000445429.1:p.Asp202Glu
ENST00000543543.5:n.1174T>G
ENST00000544182.1:n.914T>G
ENST00000544387.5:c.651+288T>G	ENSP00000438424.1:n.651+288T>G
ENST00000545621.5:c.*834T>G	ENSP00000444849.1:n.*834T>G
ENST00000546226.5:n.1227T>G
NM_000190.3:c.699T>G	NP_000181.2:p.Asp233Glu
NM_001024382.1:c.648T>G	NP_001019553.1:p.Asp216Glu
NM_001258208.1:c.651+288T>G	NP_001245137.1:n.651+288T>G
NM_001258209.1:c.600+288T>G	NP_001245138.1:n.600+288T>G
XM_005271531.1:c.648T>G	XP_005271588.1:p.Asp216Glu
XM_005271532.1:c.648T>G	XP_005271589.1:p.Asp216Glu
XM_005271533.2:c.645T>G	XP_005271590.1:p.Asp215Glu
XM_011542796.1:c.534T>G	XP_011541098.1:p.Asp178Glu
NM_000190.4:c.699T>G MANE Select	NP_000181.2:p.Asp233Glu
NM_001024382.2:c.648T>G	NP_001019553.1:p.Asp216Glu
XM_005271533.3:c.645T>G	XP_005271590.1:p.Asp215Glu
XM_017017629.1:c.648T>G	XP_016873118.1:p.Asp216Glu
XM_024448460.1:c.597+288T>G	XP_024304228.1:n.597+288T>G
NM_001258208.2:c.651+288T>G	NP_001245137.1:n.651+288T>G
NM_001258209.2:c.600+288T>G	NP_001245138.1:n.600+288T>G