Canonical Allele Identifier: CA382898050

Gene: HMBS

Linked Data

• MyVariant Identifiers: chr11:g.118963226G>T (hg19) ; chr11:g.119092516G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119092516G>T , CM000673.2:g.119092516G>T	GRCh38
NC_000011.9:g.118963226G>T , CM000673.1:g.118963226G>T	GRCh37
NC_000011.8:g.118468436G>T	NCBI36
NG_008093.1:g.12640G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000686218.1:c.599G>T	ENSP00000509288.1:p.Arg200Met
ENST00000691144.1:n.2745G>T
ENST00000691249.1:n.1588G>T
ENST00000442944.7:c.746G>T	ENSP00000392041.3:p.Arg249Met
ENST00000640813.1:c.*1G>T	ENSP00000491061.1:n.*1G>T
ENST00000648026.1:c.658G>T	ENSP00000498044.1:n.658G>T
ENST00000648374.1:c.713G>T	ENSP00000497255.1:p.Arg238Met
ENST00000649823.1:n.1221G>T
ENST00000650101.1:c.695G>T	ENSP00000496970.1:p.Arg232Met
ENST00000650307.1:n.1590G>T
ENST00000652429.1:c.764G>T MANE Select	ENSP00000498786.1:p.Arg255Met
ENST00000278715.7:c.764G>T	ENSP00000278715.3:p.Arg255Met
ENST00000392841.1:c.713G>T	ENSP00000376584.1:p.Arg238Met
ENST00000442944.6:c.713G>T	ENSP00000392041.2:p.Arg238Met
ENST00000537841.5:c.713G>T	ENSP00000444730.1:p.Arg238Met
ENST00000542044.5:n.1209G>T
ENST00000542729.5:c.601-242G>T	ENSP00000443058.1:n.601-242G>T
ENST00000543090.5:c.671G>T	ENSP00000445429.1:p.Arg224Met
ENST00000543543.5:n.1239G>T
ENST00000544182.1:n.979G>T
ENST00000544387.5:c.652-242G>T	ENSP00000438424.1:n.652-242G>T
ENST00000546226.5:n.1292G>T
NM_000190.3:c.764G>T	NP_000181.2:p.Arg255Met
NM_001024382.1:c.713G>T	NP_001019553.1:p.Arg238Met
NM_001258208.1:c.652-242G>T	NP_001245137.1:n.652-242G>T
NM_001258209.1:c.601-242G>T	NP_001245138.1:n.601-242G>T
XM_005271531.1:c.713G>T	XP_005271588.1:p.Arg238Met
XM_005271532.1:c.713G>T	XP_005271589.1:p.Arg238Met
XM_005271533.2:c.710G>T	XP_005271590.1:p.Arg237Met
XM_011542796.1:c.599G>T	XP_011541098.1:p.Arg200Met
NM_000190.4:c.764G>T MANE Select	NP_000181.2:p.Arg255Met
NM_001024382.2:c.713G>T	NP_001019553.1:p.Arg238Met
XM_005271533.3:c.710G>T	XP_005271590.1:p.Arg237Met
XM_017017629.1:c.713G>T	XP_016873118.1:p.Arg238Met
XM_024448460.1:c.598-242G>T	XP_024304228.1:n.598-242G>T
NM_001258208.2:c.652-242G>T	NP_001245137.1:n.652-242G>T
NM_001258209.2:c.601-242G>T	NP_001245138.1:n.601-242G>T