Canonical Allele Identifier: CA2397714802

Gene: BCR

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23285071T= , CM000684.2:g.23285071T=	GRCh38
NC_000022.10:g.23627258T= , CM000684.1:g.23627258T=	GRCh37
NC_000022.9:g.21957258T=	NCBI36
NG_009244.1:g.109707T=
NG_009244.2:g.109707T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305877.13:c.2276T= MANE Select	ENSP00000303507.8:p.Leu759=
ENST00000305877.12:c.2276T=	ENSP00000303507.8:p.Leu759=
ENST00000359540.7:c.2276T=	ENSP00000352535.3:p.Leu759=
ENST00000398512.9:c.1270-3073T=	ENSP00000381524.6:n.1270-3073T=
ENST00000427791.1:c.728T=	ENSP00000396531.1:p.Leu243=
ENST00000466076.1:n.350T=
ENST00000487968.5:n.929T=
NM_004327.3:c.2276T=	NP_004318.3:p.Leu759=
NM_021574.2:c.2276T=	NP_067585.2:p.Leu759=
NM_004327.4:c.2276T= MANE Select	NP_004318.3:p.Leu759=
NM_021574.3:c.2276T=	NP_067585.2:p.Leu759=