Canonical Allele Identifier: CA382897703

Gene: HMBS

Linked Data

• MyVariant Identifiers: chr11:g.118963183C>T (hg19) ; chr11:g.119092473C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119092473C>T , CM000673.2:g.119092473C>T	GRCh38
NC_000011.9:g.118963183C>T , CM000673.1:g.118963183C>T	GRCh37
NC_000011.8:g.118468393C>T	NCBI36
NG_008093.1:g.12597C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686218.1:c.556C>T	ENSP00000509288.1:p.Pro186Ser
ENST00000691144.1:n.2702C>T
ENST00000691249.1:n.1545C>T
ENST00000442944.7:c.703C>T	ENSP00000392041.3:p.Pro235Ser
ENST00000536813.6:c.670C>T	ENSP00000438726.2:p.Pro224Ser
ENST00000640813.1:c.531C>T	ENSP00000491061.1:p.Ile177=
ENST00000648026.1:c.615C>T	ENSP00000498044.1:p.Ile205=
ENST00000648374.1:c.670C>T	ENSP00000497255.1:p.Pro224Ser
ENST00000649823.1:n.1178C>T
ENST00000650101.1:c.652C>T	ENSP00000496970.1:p.Pro218Ser
ENST00000650307.1:n.1547C>T
ENST00000652429.1:c.721C>T MANE Select	ENSP00000498786.1:p.Pro241Ser
ENST00000278715.7:c.721C>T	ENSP00000278715.3:p.Pro241Ser
ENST00000392841.1:c.670C>T	ENSP00000376584.1:p.Pro224Ser
ENST00000442944.6:c.670C>T	ENSP00000392041.2:p.Pro224Ser
ENST00000537841.5:c.670C>T	ENSP00000444730.1:p.Pro224Ser
ENST00000542044.5:n.1166C>T
ENST00000542729.5:c.601-285C>T	ENSP00000443058.1:n.601-285C>T
ENST00000543090.5:c.628C>T	ENSP00000445429.1:p.Pro210Ser
ENST00000543543.5:n.1196C>T
ENST00000544182.1:n.936C>T
ENST00000544387.5:c.652-285C>T	ENSP00000438424.1:n.652-285C>T
ENST00000545621.5:c.*856C>T	ENSP00000444849.1:n.*856C>T
ENST00000546226.5:n.1249C>T
NM_000190.3:c.721C>T	NP_000181.2:p.Pro241Ser
NM_001024382.1:c.670C>T	NP_001019553.1:p.Pro224Ser
NM_001258208.1:c.652-285C>T	NP_001245137.1:n.652-285C>T
NM_001258209.1:c.601-285C>T	NP_001245138.1:n.601-285C>T
XM_005271531.1:c.670C>T	XP_005271588.1:p.Pro224Ser
XM_005271532.1:c.670C>T	XP_005271589.1:p.Pro224Ser
XM_005271533.2:c.667C>T	XP_005271590.1:p.Pro223Ser
XM_011542796.1:c.556C>T	XP_011541098.1:p.Pro186Ser
NM_000190.4:c.721C>T MANE Select	NP_000181.2:p.Pro241Ser
NM_001024382.2:c.670C>T	NP_001019553.1:p.Pro224Ser
XM_005271533.3:c.667C>T	XP_005271590.1:p.Pro223Ser
XM_017017629.1:c.670C>T	XP_016873118.1:p.Pro224Ser
XM_024448460.1:c.598-285C>T	XP_024304228.1:n.598-285C>T
NM_001258208.2:c.652-285C>T	NP_001245137.1:n.652-285C>T
NM_001258209.2:c.601-285C>T	NP_001245138.1:n.601-285C>T