Canonical Allele Identifier: CA2397725453

Gene: BCR

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23305880_23305881delinsGT , CM000684.2:g.23305880_23305881delinsGT	GRCh38
NC_000022.10:g.23648067_23648068delinsGT , CM000684.1:g.23648067_23648068delinsGT	GRCh37
NC_000022.9:g.21978067_21978068delinsGT	NCBI36
NG_009244.1:g.130516_130517delinsGT
NG_009244.2:g.130516_130517delinsGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000305877.13:c.3013-3544_3013-3543delinsGT MANE Select	ENSP00000303507.8:n.3013-3544_3013-3543delinsGT
ENST00000305877.12:c.3013-3544_3013-3543delinsGT	ENSP00000303507.8:n.3013-3544_3013-3543delinsGT
ENST00000359540.7:c.2881-3544_2881-3543delinsGT	ENSP00000352535.3:n.2881-3544_2881-3543delinsGT
ENST00000398512.9:c.1709-3544_1709-3543delinsGT	ENSP00000381524.6:n.1709-3544_1709-3543delinsGT
ENST00000419722.6:n.238-3544_238-3543delinsGT
NM_004327.3:c.3013-3544_3013-3543delinsGT	NP_004318.3:n.3013-3544_3013-3543delinsGT
NM_021574.2:c.2881-3544_2881-3543delinsGT	NP_067585.2:n.2881-3544_2881-3543delinsGT
NM_004327.4:c.3013-3544_3013-3543delinsGT MANE Select	NP_004318.3:n.3013-3544_3013-3543delinsGT
NM_021574.3:c.2881-3544_2881-3543delinsGT	NP_067585.2:n.2881-3544_2881-3543delinsGT