Canonical Allele Identifier: CA2397714818

Gene: BCR

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23285109G= , CM000684.2:g.23285109G=	GRCh38
NC_000022.10:g.23627296G= , CM000684.1:g.23627296G=	GRCh37
NC_000022.9:g.21957296G=	NCBI36
NG_009244.1:g.109745G=
NG_009244.2:g.109745G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305877.13:c.2314G= MANE Select	ENSP00000303507.8:p.Ala772=
ENST00000305877.12:c.2314G=	ENSP00000303507.8:p.Ala772=
ENST00000359540.7:c.2314G=	ENSP00000352535.3:p.Ala772=
ENST00000398512.9:c.1270-3035G=	ENSP00000381524.6:n.1270-3035G=
ENST00000427791.1:c.766G=	ENSP00000396531.1:p.Ala256=
ENST00000466076.1:n.388G=
ENST00000487968.5:n.967G=
NM_004327.3:c.2314G=	NP_004318.3:p.Ala772=
NM_021574.2:c.2314G=	NP_067585.2:p.Ala772=
NM_004327.4:c.2314G= MANE Select	NP_004318.3:p.Ala772=
NM_021574.3:c.2314G=	NP_067585.2:p.Ala772=