Canonical Allele Identifier: CA382898920

Gene: HMBS

Linked Data

• gnomAD v4: 11-119092999-C-G
• MyVariant Identifiers: chr11:g.118963709C>G (hg19) ; chr11:g.119092999C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119092999C>G , CM000673.2:g.119092999C>G	GRCh38
NC_000011.9:g.118963709C>G , CM000673.1:g.118963709C>G	GRCh37
NC_000011.8:g.118468919C>G	NCBI36
NG_008093.1:g.13123C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686218.1:c.725C>G	ENSP00000509288.1:p.Ala242Gly
ENST00000691144.1:n.3105C>G
ENST00000691249.1:n.1714C>G
ENST00000442944.7:c.872C>G	ENSP00000392041.3:p.Ala291Gly
ENST00000640813.1:c.*127C>G	ENSP00000491061.1:n.*127C>G
ENST00000648026.1:c.784C>G	ENSP00000498044.1:n.784C>G
ENST00000648374.1:c.839C>G	ENSP00000497255.1:p.Ala280Gly
ENST00000650101.1:c.821C>G	ENSP00000496970.1:p.Ala274Gly
ENST00000650307.1:n.1716C>G
ENST00000652429.1:c.890C>G MANE Select	ENSP00000498786.1:p.Ala297Gly
ENST00000278715.7:c.890C>G	ENSP00000278715.3:p.Ala297Gly
ENST00000392841.1:c.839C>G	ENSP00000376584.1:p.Ala280Gly
ENST00000442944.6:c.839C>G	ENSP00000392041.2:p.Ala280Gly
ENST00000537841.5:c.839C>G	ENSP00000444730.1:p.Ala280Gly
ENST00000539045.1:n.389C>G
ENST00000542044.5:n.1335C>G
ENST00000542729.5:c.719C>G	ENSP00000443058.1:p.Ala240Gly
ENST00000543090.5:c.797C>G	ENSP00000445429.1:p.Ala266Gly
ENST00000543543.5:n.1365C>G
ENST00000544182.1:n.1339C>G
ENST00000544387.5:c.770C>G	ENSP00000438424.1:p.Ala257Gly
ENST00000546226.5:n.1652C>G
NM_000190.3:c.890C>G	NP_000181.2:p.Ala297Gly
NM_001024382.1:c.839C>G	NP_001019553.1:p.Ala280Gly
NM_001258208.1:c.770C>G	NP_001245137.1:p.Ala257Gly
NM_001258209.1:c.719C>G	NP_001245138.1:p.Ala240Gly
XM_005271531.1:c.839C>G	XP_005271588.1:p.Ala280Gly
XM_005271532.1:c.839C>G	XP_005271589.1:p.Ala280Gly
XM_005271533.2:c.836C>G	XP_005271590.1:p.Ala279Gly
XM_011542796.1:c.725C>G	XP_011541098.1:p.Ala242Gly
NM_000190.4:c.890C>G MANE Select	NP_000181.2:p.Ala297Gly
NM_001024382.2:c.839C>G	NP_001019553.1:p.Ala280Gly
XM_005271533.3:c.836C>G	XP_005271590.1:p.Ala279Gly
XM_017017629.1:c.839C>G	XP_016873118.1:p.Ala280Gly
XM_024448460.1:c.716C>G	XP_024304228.1:p.Ala239Gly
NM_001258208.2:c.770C>G	NP_001245137.1:p.Ala257Gly
NM_001258209.2:c.719C>G	NP_001245138.1:p.Ala240Gly