Canonical Allele Identifier: CA477369341

Gene: HMBS

Linked Data

• MyVariant Identifiers: chr11:g.118963915C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119093205C>A , CM000673.2:g.119093205C>A	GRCh38
NC_000011.9:g.118963915C>A , CM000673.1:g.118963915C>A	GRCh37
NC_000011.8:g.118469125C>A	NCBI36
NG_008093.1:g.13329C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686218.1:c.843C>A	ENSP00000509288.1:p.Ile281=
ENST00000691144.1:n.3223C>A
ENST00000691249.1:n.1832C>A
ENST00000442944.7:c.990C>A	ENSP00000392041.3:p.Ile330=
ENST00000640813.1:c.*245C>A	ENSP00000491061.1:n.*245C>A
ENST00000648026.1:c.902C>A	ENSP00000498044.1:n.902C>A
ENST00000648374.1:c.957C>A	ENSP00000497255.1:p.Ile319=
ENST00000650101.1:c.939C>A	ENSP00000496970.1:p.Ile313=
ENST00000650307.1:n.1834C>A
ENST00000652429.1:c.1008C>A MANE Select	ENSP00000498786.1:p.Ile336=
ENST00000278715.7:c.1008C>A	ENSP00000278715.3:p.Ile336=
ENST00000392841.1:c.957C>A	ENSP00000376584.1:p.Ile319=
ENST00000442944.6:c.957C>A	ENSP00000392041.2:p.Ile319=
ENST00000537841.5:c.957C>A	ENSP00000444730.1:p.Ile319=
ENST00000539045.1:n.507C>A
ENST00000542044.5:n.1453C>A
ENST00000542729.5:c.837C>A	ENSP00000443058.1:p.Ile279=
ENST00000543090.5:c.915C>A	ENSP00000445429.1:p.Ile305=
ENST00000543543.5:n.1483C>A
ENST00000544182.1:n.1457C>A
ENST00000544387.5:c.888C>A	ENSP00000438424.1:p.Ile296=
ENST00000546226.5:n.1770C>A
NM_000190.3:c.1008C>A	NP_000181.2:p.Ile336=
NM_001024382.1:c.957C>A	NP_001019553.1:p.Ile319=
NM_001258208.1:c.888C>A	NP_001245137.1:p.Ile296=
NM_001258209.1:c.837C>A	NP_001245138.1:p.Ile279=
XM_005271531.1:c.957C>A	XP_005271588.1:p.Ile319=
XM_005271532.1:c.957C>A	XP_005271589.1:p.Ile319=
XM_005271533.2:c.954C>A	XP_005271590.1:p.Ile318=
XM_011542796.1:c.843C>A	XP_011541098.1:p.Ile281=
NM_000190.4:c.1008C>A MANE Select	NP_000181.2:p.Ile336=
NM_001024382.2:c.957C>A	NP_001019553.1:p.Ile319=
XM_005271533.3:c.954C>A	XP_005271590.1:p.Ile318=
XM_017017629.1:c.957C>A	XP_016873118.1:p.Ile319=
XM_024448460.1:c.834C>A	XP_024304228.1:p.Ile278=
NM_001258208.2:c.888C>A	NP_001245137.1:p.Ile296=
NM_001258209.2:c.837C>A	NP_001245138.1:p.Ile279=