Canonical Allele Identifier: CA382628608

Gene: BCO2

Linked Data

• gnomAD v4: 11-112193650-T-A
• MyVariant Identifiers: chr11:g.112064373T>A (hg19) ; chr11:g.112193650T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112193650T>A , CM000673.2:g.112193650T>A	GRCh38
NC_000011.9:g.112064373T>A , CM000673.1:g.112064373T>A	GRCh37
NC_000011.8:g.111569583T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357685.11:c.470T>A MANE Select	ENSP00000350314.5:p.Val157Asp
ENST00000357685.9:c.470T>A	ENSP00000350314.5:p.Val157Asp
ENST00000361053.8:c.470T>A	ENSP00000354338.4:p.Val157Asp
ENST00000438022.5:c.368T>A	ENSP00000414843.1:p.Val123Asp
ENST00000460924.6:n.562T>A
ENST00000494860.5:n.322T>A
ENST00000525987.5:n.813T>A
ENST00000526088.5:c.368T>A	ENSP00000436615.1:p.Val123Asp
ENST00000527939.1:c.*112T>A	ENSP00000436956.1:n.*112T>A
ENST00000530677.1:c.177T>A
ENST00000531169.5:c.368T>A	ENSP00000437053.1:p.Val123Asp
ENST00000532593.5:c.155T>A	ENSP00000431802.1:p.Val52Asp
ENST00000532612.5:c.400T>A
ENST00000534122.5:n.1085T>A
ENST00000534550.5:c.*112T>A	ENSP00000434488.1:n.*112T>A
NM_001037290.2:c.368T>A	NP_001032367.2:p.Val123Asp
NM_001256397.1:c.368T>A	NP_001243326.1:p.Val123Asp
NM_001256398.1:c.470T>A	NP_001243327.1:p.Val157Asp
NM_001256400.1:c.155T>A	NP_001243329.1:p.Val52Asp
NM_031938.5:c.470T>A	NP_114144.4:p.Val157Asp
NM_001037290.3:c.368T>A	NP_001032367.3:p.Val123Asp
NM_001256397.2:c.368T>A	NP_001243326.2:p.Val123Asp
NM_001256398.2:c.470T>A	NP_001243327.2:p.Val157Asp
NM_001256400.2:c.155T>A	NP_001243329.2:p.Val52Asp
NM_031938.7:c.470T>A MANE Select	NP_114144.5:p.Val157Asp
NM_001037290.4:c.368T>A	NP_001032367.3:p.Val123Asp
NM_001256397.3:c.368T>A	NP_001243326.2:p.Val123Asp
NM_001256398.3:c.470T>A	NP_001243327.2:p.Val157Asp
NM_001256400.3:c.155T>A	NP_001243329.2:p.Val52Asp