Canonical Allele Identifier: CA2000603770

Gene: BCO2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112193515T= , CM000673.2:g.112193515T=	GRCh38
NC_000011.9:g.112064238T= , CM000673.1:g.112064238T=	GRCh37
NC_000011.8:g.111569448T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357685.11:c.335T= MANE Select	ENSP00000350314.5:p.Phe112=
ENST00000357685.9:c.335T=	ENSP00000350314.5:p.Phe112=
ENST00000361053.8:c.335T=	ENSP00000354338.4:p.Phe112=
ENST00000438022.5:c.233T=	ENSP00000414843.1:p.Phe78=
ENST00000460924.6:n.427T=
ENST00000494860.5:n.187T=
ENST00000525468.1:n.324T=
ENST00000525987.5:n.678T=
ENST00000526088.5:c.233T=	ENSP00000436615.1:p.Phe78=
ENST00000527939.1:c.130T=	ENSP00000436956.1:p.Ser44=
ENST00000530677.1:c.42T=
ENST00000531003.1:c.*125T=	ENSP00000435869.1:n.*125T=
ENST00000531169.5:c.233T=	ENSP00000437053.1:p.Phe78=
ENST00000532593.5:c.20T=	ENSP00000431802.1:p.Phe7=
ENST00000532612.5:c.265T=
ENST00000532699.1:c.*97T=	ENSP00000456434.1:n.*97T=
ENST00000534122.5:n.950T=
ENST00000534550.5:c.130T=	ENSP00000434488.1:p.Ser44=
NM_001037290.2:c.233T=	NP_001032367.2:p.Phe78=
NM_001256397.1:c.233T=	NP_001243326.1:p.Phe78=
NM_001256398.1:c.335T=	NP_001243327.1:p.Phe112=
NM_001256400.1:c.20T=	NP_001243329.1:p.Phe7=
NM_031938.5:c.335T=	NP_114144.4:p.Phe112=
NM_001037290.3:c.233T=	NP_001032367.3:p.Phe78=
NM_001256397.2:c.233T=	NP_001243326.2:p.Phe78=
NM_001256398.2:c.335T=	NP_001243327.2:p.Phe112=
NM_001256400.2:c.20T=	NP_001243329.2:p.Phe7=
NM_031938.7:c.335T= MANE Select	NP_114144.5:p.Phe112=
NM_001037290.4:c.233T=	NP_001032367.3:p.Phe78=
NM_001256397.3:c.233T=	NP_001243326.2:p.Phe78=
NM_001256398.3:c.335T=	NP_001243327.2:p.Phe112=
NM_001256400.3:c.20T=	NP_001243329.2:p.Phe7=