Canonical Allele Identifier: CA410896972

Gene: BCR

Linked Data

• COSMIC: COSM6094963
• MyVariant Identifiers: chr22:g.23627343G>C (hg19) ; chr22:g.23285156G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23285156G>C , CM000684.2:g.23285156G>C	GRCh38
NC_000022.10:g.23627343G>C , CM000684.1:g.23627343G>C	GRCh37
NC_000022.9:g.21957343G>C	NCBI36
NG_009244.1:g.109792G>C
NG_009244.2:g.109792G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305877.13:c.2361G>C MANE Select	ENSP00000303507.8:p.Leu787Phe
ENST00000305877.12:c.2361G>C	ENSP00000303507.8:p.Leu787Phe
ENST00000359540.7:c.2361G>C	ENSP00000352535.3:p.Leu787Phe
ENST00000398512.9:c.1270-2988G>C	ENSP00000381524.6:n.1270-2988G>C
ENST00000466076.1:n.435G>C
ENST00000487968.5:n.1014G>C
NM_004327.3:c.2361G>C	NP_004318.3:p.Leu787Phe
NM_021574.2:c.2361G>C	NP_067585.2:p.Leu787Phe
NM_004327.4:c.2361G>C MANE Select	NP_004318.3:p.Leu787Phe
NM_021574.3:c.2361G>C	NP_067585.2:p.Leu787Phe