Canonical Allele Identifier: CA382628799

Gene: BCO2

Linked Data

• MyVariant Identifiers: chr11:g.112064632T>G (hg19) ; chr11:g.112193909T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112193909T>G , CM000673.2:g.112193909T>G	GRCh38
NC_000011.9:g.112064632T>G , CM000673.1:g.112064632T>G	GRCh37
NC_000011.8:g.111569842T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357685.11:c.548T>G MANE Select	ENSP00000350314.5:p.Val183Gly
ENST00000357685.9:c.548T>G	ENSP00000350314.5:p.Val183Gly
ENST00000361053.8:c.517+212T>G	ENSP00000354338.4:n.517+212T>G
ENST00000438022.5:c.446T>G	ENSP00000414843.1:p.Val149Gly
ENST00000460924.6:n.821T>G
ENST00000494860.5:n.581T>G
ENST00000526088.5:c.446T>G	ENSP00000436615.1:p.Val149Gly
ENST00000527939.1:c.*190T>G	ENSP00000436956.1:n.*190T>G
ENST00000530677.1:c.243T>G
ENST00000531169.5:c.446T>G	ENSP00000437053.1:p.Val149Gly
ENST00000532593.5:c.233T>G	ENSP00000431802.1:p.Val78Gly
ENST00000532612.5:c.447+212T>G
ENST00000534550.5:c.*159+212T>G	ENSP00000434488.1:n.*159+212T>G
NM_001037290.2:c.446T>G	NP_001032367.2:p.Val149Gly
NM_001256397.1:c.446T>G	NP_001243326.1:p.Val149Gly
NM_001256398.1:c.517+212T>G	NP_001243327.1:n.517+212T>G
NM_001256400.1:c.233T>G	NP_001243329.1:p.Val78Gly
NM_031938.5:c.548T>G	NP_114144.4:p.Val183Gly
NM_001037290.3:c.446T>G	NP_001032367.3:p.Val149Gly
NM_001256397.2:c.446T>G	NP_001243326.2:p.Val149Gly
NM_001256398.2:c.517+212T>G	NP_001243327.2:n.517+212T>G
NM_001256400.2:c.233T>G	NP_001243329.2:p.Val78Gly
NM_031938.7:c.548T>G MANE Select	NP_114144.5:p.Val183Gly
NM_001037290.4:c.446T>G	NP_001032367.3:p.Val149Gly
NM_001256397.3:c.446T>G	NP_001243326.2:p.Val149Gly
NM_001256398.3:c.517+212T>G	NP_001243327.2:n.517+212T>G
NM_001256400.3:c.233T>G	NP_001243329.2:p.Val78Gly