Canonical Allele Identifier: CA382899168

Gene: HMBS

Linked Data

• MyVariant Identifiers: chr11:g.118963845C>G (hg19) ; chr11:g.119093135C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119093135C>G , CM000673.2:g.119093135C>G	GRCh38
NC_000011.9:g.118963845C>G , CM000673.1:g.118963845C>G	GRCh37
NC_000011.8:g.118469055C>G	NCBI36
NG_008093.1:g.13259C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686218.1:c.773C>G	ENSP00000509288.1:p.Pro258Arg
ENST00000691144.1:n.3153C>G
ENST00000691249.1:n.1762C>G
ENST00000442944.7:c.920C>G	ENSP00000392041.3:p.Pro307Arg
ENST00000640813.1:c.*175C>G	ENSP00000491061.1:n.*175C>G
ENST00000648026.1:c.832C>G	ENSP00000498044.1:n.832C>G
ENST00000648374.1:c.887C>G	ENSP00000497255.1:p.Pro296Arg
ENST00000650101.1:c.869C>G	ENSP00000496970.1:p.Pro290Arg
ENST00000650307.1:n.1764C>G
ENST00000652429.1:c.938C>G MANE Select	ENSP00000498786.1:p.Pro313Arg
ENST00000278715.7:c.938C>G	ENSP00000278715.3:p.Pro313Arg
ENST00000392841.1:c.887C>G	ENSP00000376584.1:p.Pro296Arg
ENST00000442944.6:c.887C>G	ENSP00000392041.2:p.Pro296Arg
ENST00000537841.5:c.887C>G	ENSP00000444730.1:p.Pro296Arg
ENST00000539045.1:n.437C>G
ENST00000542044.5:n.1383C>G
ENST00000542729.5:c.767C>G	ENSP00000443058.1:p.Pro256Arg
ENST00000543090.5:c.845C>G	ENSP00000445429.1:p.Pro282Arg
ENST00000543543.5:n.1413C>G
ENST00000544182.1:n.1387C>G
ENST00000544387.5:c.818C>G	ENSP00000438424.1:p.Pro273Arg
ENST00000546226.5:n.1700C>G
NM_000190.3:c.938C>G	NP_000181.2:p.Pro313Arg
NM_001024382.1:c.887C>G	NP_001019553.1:p.Pro296Arg
NM_001258208.1:c.818C>G	NP_001245137.1:p.Pro273Arg
NM_001258209.1:c.767C>G	NP_001245138.1:p.Pro256Arg
XM_005271531.1:c.887C>G	XP_005271588.1:p.Pro296Arg
XM_005271532.1:c.887C>G	XP_005271589.1:p.Pro296Arg
XM_005271533.2:c.884C>G	XP_005271590.1:p.Pro295Arg
XM_011542796.1:c.773C>G	XP_011541098.1:p.Pro258Arg
NM_000190.4:c.938C>G MANE Select	NP_000181.2:p.Pro313Arg
NM_001024382.2:c.887C>G	NP_001019553.1:p.Pro296Arg
XM_005271533.3:c.884C>G	XP_005271590.1:p.Pro295Arg
XM_017017629.1:c.887C>G	XP_016873118.1:p.Pro296Arg
XM_024448460.1:c.764C>G	XP_024304228.1:p.Pro255Arg
NM_001258208.2:c.818C>G	NP_001245137.1:p.Pro273Arg
NM_001258209.2:c.767C>G	NP_001245138.1:p.Pro256Arg