Canonical Allele Identifier: CA2397680754

Gene: BCR

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23216392A= , CM000684.2:g.23216392A=	GRCh38
NC_000022.10:g.23558579A= , CM000684.1:g.23558579A=	GRCh37
NC_000022.9:g.21888579A=	NCBI36
NG_009244.1:g.41028A=
NG_009244.2:g.41028A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000305877.13:c.1279+34153A= MANE Select	ENSP00000303507.8:n.1279+34153A=
ENST00000305877.12:c.1279+34153A=	ENSP00000303507.8:n.1279+34153A=
ENST00000359540.7:c.1279+34153A=	ENSP00000352535.3:n.1279+34153A=
ENST00000398512.9:c.1269+34163A=	ENSP00000381524.6:n.1269+34163A=
ENST00000463770.5:n.133+18007A=
ENST00000479188.5:n.130-26426A=
ENST00000487679.1:n.196+17040A=
NM_004327.3:c.1279+34153A=	NP_004318.3:n.1279+34153A=
NM_021574.2:c.1279+34153A=	NP_067585.2:n.1279+34153A=
NM_004327.4:c.1279+34153A= MANE Select	NP_004318.3:n.1279+34153A=
NM_021574.3:c.1279+34153A=	NP_067585.2:n.1279+34153A=