Canonical Allele Identifier: CA2397674401

Gene: BCR

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23203802C= , CM000684.2:g.23203802C=	GRCh38
NC_000022.10:g.23545989C= , CM000684.1:g.23545989C=	GRCh37
NC_000022.9:g.21875989C=	NCBI36
NG_009244.1:g.28438C=
NG_009244.2:g.28438C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305877.13:c.1279+21563C= MANE Select	ENSP00000303507.8:n.1279+21563C=
ENST00000305877.12:c.1279+21563C=	ENSP00000303507.8:n.1279+21563C=
ENST00000359540.7:c.1279+21563C=	ENSP00000352535.3:n.1279+21563C=
ENST00000398512.9:c.1269+21573C=	ENSP00000381524.6:n.1269+21573C=
ENST00000463770.5:n.133+5417C=
ENST00000479188.5:n.129+23970C=
ENST00000487679.1:n.196+4450C=
NM_004327.3:c.1279+21563C=	NP_004318.3:n.1279+21563C=
NM_021574.2:c.1279+21563C=	NP_067585.2:n.1279+21563C=
NM_004327.4:c.1279+21563C= MANE Select	NP_004318.3:n.1279+21563C=
NM_021574.3:c.1279+21563C=	NP_067585.2:n.1279+21563C=