Canonical Allele Identifier: CA2000603833

Gene: BCO2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112193665T= , CM000673.2:g.112193665T=	GRCh38
NC_000011.9:g.112064388T= , CM000673.1:g.112064388T=	GRCh37
NC_000011.8:g.111569598T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357685.11:c.485T= MANE Select	ENSP00000350314.5:p.Met162=
ENST00000357685.9:c.485T=	ENSP00000350314.5:p.Met162=
ENST00000361053.8:c.485T=	ENSP00000354338.4:p.Met162=
ENST00000438022.5:c.383T=	ENSP00000414843.1:p.Met128=
ENST00000460924.6:n.577T=
ENST00000494860.5:n.337T=
ENST00000525987.5:n.828T=
ENST00000526088.5:c.383T=	ENSP00000436615.1:p.Met128=
ENST00000527939.1:c.*127T=	ENSP00000436956.1:n.*127T=
ENST00000530677.1:c.192T=
ENST00000531169.5:c.383T=	ENSP00000437053.1:p.Met128=
ENST00000532593.5:c.170T=	ENSP00000431802.1:p.Met57=
ENST00000532612.5:c.415T=
ENST00000534122.5:n.1100T=
ENST00000534550.5:c.*127T=	ENSP00000434488.1:n.*127T=
NM_001037290.2:c.383T=	NP_001032367.2:p.Met128=
NM_001256397.1:c.383T=	NP_001243326.1:p.Met128=
NM_001256398.1:c.485T=	NP_001243327.1:p.Met162=
NM_001256400.1:c.170T=	NP_001243329.1:p.Met57=
NM_031938.5:c.485T=	NP_114144.4:p.Met162=
NM_001037290.3:c.383T=	NP_001032367.3:p.Met128=
NM_001256397.2:c.383T=	NP_001243326.2:p.Met128=
NM_001256398.2:c.485T=	NP_001243327.2:p.Met162=
NM_001256400.2:c.170T=	NP_001243329.2:p.Met57=
NM_031938.7:c.485T= MANE Select	NP_114144.5:p.Met162=
NM_001037290.4:c.383T=	NP_001032367.3:p.Met128=
NM_001256397.3:c.383T=	NP_001243326.2:p.Met128=
NM_001256398.3:c.485T=	NP_001243327.2:p.Met162=
NM_001256400.3:c.170T=	NP_001243329.2:p.Met57=