Canonical Allele Identifier: CA2842111813

Gene: BCR

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23285146dup , CM000684.2:g.23285146dup	GRCh38
NC_000022.10:g.23627333dup , CM000684.1:g.23627333dup	GRCh37
NC_000022.9:g.21957333dup	NCBI36
NG_009244.1:g.109782dup
NG_009244.2:g.109782dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305877.13:c.2351dup MANE Select	ENSP00000303507.8:p.Asp785GlyfsTer13
ENST00000305877.12:c.2351dup	ENSP00000303507.8:p.Asp785GlyfsTer13
ENST00000359540.7:c.2351dup	ENSP00000352535.3:p.Asp785GlyfsTer13
ENST00000398512.9:c.1270-2998dup	ENSP00000381524.6:n.1270-2998dup
ENST00000466076.1:n.425dup
ENST00000487968.5:n.1004dup
NM_004327.3:c.2351dup	NP_004318.3:p.Asp785GlyfsTer13
NM_021574.2:c.2351dup	NP_067585.2:p.Asp785GlyfsTer13
NM_004327.4:c.2351dup MANE Select	NP_004318.3:p.Asp785GlyfsTer13
NM_021574.3:c.2351dup	NP_067585.2:p.Asp785GlyfsTer13