Canonical Allele Identifier: CA382628674

Gene: BCO2

Linked Data

• MyVariant Identifiers: chr11:g.112064400A>T (hg19) ; chr11:g.112193677A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112193677A>T , CM000673.2:g.112193677A>T	GRCh38
NC_000011.9:g.112064400A>T , CM000673.1:g.112064400A>T	GRCh37
NC_000011.8:g.111569610A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357685.11:c.497A>T MANE Select	ENSP00000350314.5:p.Glu166Val
ENST00000357685.9:c.497A>T	ENSP00000350314.5:p.Glu166Val
ENST00000361053.8:c.497A>T	ENSP00000354338.4:p.Glu166Val
ENST00000438022.5:c.395A>T	ENSP00000414843.1:p.Glu132Val
ENST00000460924.6:n.589A>T
ENST00000494860.5:n.349A>T
ENST00000525987.5:n.840A>T
ENST00000526088.5:c.395A>T	ENSP00000436615.1:p.Glu132Val
ENST00000527939.1:c.*139A>T	ENSP00000436956.1:n.*139A>T
ENST00000530677.1:c.204A>T
ENST00000531169.5:c.395A>T	ENSP00000437053.1:p.Glu132Val
ENST00000532593.5:c.182A>T	ENSP00000431802.1:p.Glu61Val
ENST00000532612.5:c.427A>T
ENST00000534122.5:n.1112A>T
ENST00000534550.5:c.*139A>T	ENSP00000434488.1:n.*139A>T
NM_001037290.2:c.395A>T	NP_001032367.2:p.Glu132Val
NM_001256397.1:c.395A>T	NP_001243326.1:p.Glu132Val
NM_001256398.1:c.497A>T	NP_001243327.1:p.Glu166Val
NM_001256400.1:c.182A>T	NP_001243329.1:p.Glu61Val
NM_031938.5:c.497A>T	NP_114144.4:p.Glu166Val
NM_001037290.3:c.395A>T	NP_001032367.3:p.Glu132Val
NM_001256397.2:c.395A>T	NP_001243326.2:p.Glu132Val
NM_001256398.2:c.497A>T	NP_001243327.2:p.Glu166Val
NM_001256400.2:c.182A>T	NP_001243329.2:p.Glu61Val
NM_031938.7:c.497A>T MANE Select	NP_114144.5:p.Glu166Val
NM_001037290.4:c.395A>T	NP_001032367.3:p.Glu132Val
NM_001256397.3:c.395A>T	NP_001243326.2:p.Glu132Val
NM_001256398.3:c.497A>T	NP_001243327.2:p.Glu166Val
NM_001256400.3:c.182A>T	NP_001243329.2:p.Glu61Val