Canonical Allele Identifier: CA477128395

Gene: HMBS

Linked Data

• MyVariant Identifiers: chr11:g.118963176G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119092466G>T , CM000673.2:g.119092466G>T	GRCh38
NC_000011.9:g.118963176G>T , CM000673.1:g.118963176G>T	GRCh37
NC_000011.8:g.118468386G>T	NCBI36
NG_008093.1:g.12590G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686218.1:c.549G>T	ENSP00000509288.1:p.Leu183=
ENST00000691144.1:n.2695G>T
ENST00000691249.1:n.1538G>T
ENST00000442944.7:c.696G>T	ENSP00000392041.3:p.Leu232=
ENST00000536813.6:c.663G>T	ENSP00000438726.2:p.Leu221=
ENST00000640813.1:c.524G>T	ENSP00000491061.1:p.Cys175Phe
ENST00000648026.1:c.608G>T	ENSP00000498044.1:p.Cys203Phe
ENST00000648374.1:c.663G>T	ENSP00000497255.1:p.Leu221=
ENST00000649823.1:n.1171G>T
ENST00000650101.1:c.645G>T	ENSP00000496970.1:p.Leu215=
ENST00000650307.1:n.1540G>T
ENST00000652429.1:c.714G>T MANE Select	ENSP00000498786.1:p.Leu238=
ENST00000278715.7:c.714G>T	ENSP00000278715.3:p.Leu238=
ENST00000392841.1:c.663G>T	ENSP00000376584.1:p.Leu221=
ENST00000442944.6:c.663G>T	ENSP00000392041.2:p.Leu221=
ENST00000537841.5:c.663G>T	ENSP00000444730.1:p.Leu221=
ENST00000542044.5:n.1159G>T
ENST00000542729.5:c.601-292G>T	ENSP00000443058.1:n.601-292G>T
ENST00000543090.5:c.621G>T	ENSP00000445429.1:p.Leu207=
ENST00000543543.5:n.1189G>T
ENST00000544182.1:n.929G>T
ENST00000544387.5:c.652-292G>T	ENSP00000438424.1:n.652-292G>T
ENST00000545621.5:c.*849G>T	ENSP00000444849.1:n.*849G>T
ENST00000546226.5:n.1242G>T
NM_000190.3:c.714G>T	NP_000181.2:p.Leu238=
NM_001024382.1:c.663G>T	NP_001019553.1:p.Leu221=
NM_001258208.1:c.652-292G>T	NP_001245137.1:n.652-292G>T
NM_001258209.1:c.601-292G>T	NP_001245138.1:n.601-292G>T
XM_005271531.1:c.663G>T	XP_005271588.1:p.Leu221=
XM_005271532.1:c.663G>T	XP_005271589.1:p.Leu221=
XM_005271533.2:c.660G>T	XP_005271590.1:p.Leu220=
XM_011542796.1:c.549G>T	XP_011541098.1:p.Leu183=
NM_000190.4:c.714G>T MANE Select	NP_000181.2:p.Leu238=
NM_001024382.2:c.663G>T	NP_001019553.1:p.Leu221=
XM_005271533.3:c.660G>T	XP_005271590.1:p.Leu220=
XM_017017629.1:c.663G>T	XP_016873118.1:p.Leu221=
XM_024448460.1:c.598-292G>T	XP_024304228.1:n.598-292G>T
NM_001258208.2:c.652-292G>T	NP_001245137.1:n.652-292G>T
NM_001258209.2:c.601-292G>T	NP_001245138.1:n.601-292G>T