Canonical Allele Identifier: CA382628374

Gene: BCO2

Linked Data

• MyVariant Identifiers: chr11:g.112064267A>T (hg19) ; chr11:g.112193544A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112193544A>T , CM000673.2:g.112193544A>T	GRCh38
NC_000011.9:g.112064267A>T , CM000673.1:g.112064267A>T	GRCh37
NC_000011.8:g.111569477A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357685.11:c.364A>T MANE Select	ENSP00000350314.5:p.Arg122Trp
ENST00000357685.9:c.364A>T	ENSP00000350314.5:p.Arg122Trp
ENST00000361053.8:c.364A>T	ENSP00000354338.4:p.Arg122Trp
ENST00000438022.5:c.262A>T	ENSP00000414843.1:p.Arg88Trp
ENST00000460924.6:n.456A>T
ENST00000494860.5:n.216A>T
ENST00000525468.1:n.353A>T
ENST00000525987.5:n.707A>T
ENST00000526088.5:c.262A>T	ENSP00000436615.1:p.Arg88Trp
ENST00000527939.1:c.*6A>T	ENSP00000436956.1:n.*6A>T
ENST00000530677.1:c.71A>T
ENST00000531169.5:c.262A>T	ENSP00000437053.1:p.Arg88Trp
ENST00000532593.5:c.49A>T	ENSP00000431802.1:p.Arg17Trp
ENST00000532612.5:c.294A>T
ENST00000532699.1:c.*126A>T	ENSP00000456434.1:n.*126A>T
ENST00000534122.5:n.979A>T
ENST00000534550.5:c.*6A>T	ENSP00000434488.1:n.*6A>T
NM_001037290.2:c.262A>T	NP_001032367.2:p.Arg88Trp
NM_001256397.1:c.262A>T	NP_001243326.1:p.Arg88Trp
NM_001256398.1:c.364A>T	NP_001243327.1:p.Arg122Trp
NM_001256400.1:c.49A>T	NP_001243329.1:p.Arg17Trp
NM_031938.5:c.364A>T	NP_114144.4:p.Arg122Trp
NM_001037290.3:c.262A>T	NP_001032367.3:p.Arg88Trp
NM_001256397.2:c.262A>T	NP_001243326.2:p.Arg88Trp
NM_001256398.2:c.364A>T	NP_001243327.2:p.Arg122Trp
NM_001256400.2:c.49A>T	NP_001243329.2:p.Arg17Trp
NM_031938.7:c.364A>T MANE Select	NP_114144.5:p.Arg122Trp
NM_001037290.4:c.262A>T	NP_001032367.3:p.Arg88Trp
NM_001256397.3:c.262A>T	NP_001243326.2:p.Arg88Trp
NM_001256398.3:c.364A>T	NP_001243327.2:p.Arg122Trp
NM_001256400.3:c.49A>T	NP_001243329.2:p.Arg17Trp