Canonical Allele Identifier: CA382898855

Gene: HMBS

Linked Data

• MyVariant Identifiers: chr11:g.118963695A>C (hg19) ; chr11:g.119092985A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119092985A>C , CM000673.2:g.119092985A>C	GRCh38
NC_000011.9:g.118963695A>C , CM000673.1:g.118963695A>C	GRCh37
NC_000011.8:g.118468905A>C	NCBI36
NG_008093.1:g.13109A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686218.1:c.711A>C	ENSP00000509288.1:p.Gln237His
ENST00000691144.1:n.3091A>C
ENST00000691249.1:n.1700A>C
ENST00000442944.7:c.858A>C	ENSP00000392041.3:p.Gln286His
ENST00000640813.1:c.*113A>C	ENSP00000491061.1:n.*113A>C
ENST00000648026.1:c.770A>C	ENSP00000498044.1:n.770A>C
ENST00000648374.1:c.825A>C	ENSP00000497255.1:p.Gln275His
ENST00000650101.1:c.807A>C	ENSP00000496970.1:p.Gln269His
ENST00000650307.1:n.1702A>C
ENST00000652429.1:c.876A>C MANE Select	ENSP00000498786.1:p.Gln292His
ENST00000278715.7:c.876A>C	ENSP00000278715.3:p.Gln292His
ENST00000392841.1:c.825A>C	ENSP00000376584.1:p.Gln275His
ENST00000442944.6:c.825A>C	ENSP00000392041.2:p.Gln275His
ENST00000537841.5:c.825A>C	ENSP00000444730.1:p.Gln275His
ENST00000539045.1:n.375A>C
ENST00000542044.5:n.1321A>C
ENST00000542729.5:c.705A>C	ENSP00000443058.1:p.Gln235His
ENST00000543090.5:c.783A>C	ENSP00000445429.1:p.Gln261His
ENST00000543543.5:n.1351A>C
ENST00000544182.1:n.1325A>C
ENST00000544387.5:c.756A>C	ENSP00000438424.1:p.Gln252His
ENST00000546226.5:n.1638A>C
NM_000190.3:c.876A>C	NP_000181.2:p.Gln292His
NM_001024382.1:c.825A>C	NP_001019553.1:p.Gln275His
NM_001258208.1:c.756A>C	NP_001245137.1:p.Gln252His
NM_001258209.1:c.705A>C	NP_001245138.1:p.Gln235His
XM_005271531.1:c.825A>C	XP_005271588.1:p.Gln275His
XM_005271532.1:c.825A>C	XP_005271589.1:p.Gln275His
XM_005271533.2:c.822A>C	XP_005271590.1:p.Gln274His
XM_011542796.1:c.711A>C	XP_011541098.1:p.Gln237His
NM_000190.4:c.876A>C MANE Select	NP_000181.2:p.Gln292His
NM_001024382.2:c.825A>C	NP_001019553.1:p.Gln275His
XM_005271533.3:c.822A>C	XP_005271590.1:p.Gln274His
XM_017017629.1:c.825A>C	XP_016873118.1:p.Gln275His
XM_024448460.1:c.702A>C	XP_024304228.1:p.Gln234His
NM_001258208.2:c.756A>C	NP_001245137.1:p.Gln252His
NM_001258209.2:c.705A>C	NP_001245138.1:p.Gln235His