Canonical Allele Identifier: CA2397725385

Gene: BCR

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23305726_23305730delinsGGGGA , CM000684.2:g.23305726_23305730delinsGGGGA	GRCh38
NC_000022.10:g.23647913_23647917delinsGGGGA , CM000684.1:g.23647913_23647917delinsGGGGA	GRCh37
NC_000022.9:g.21977913_21977917delinsGGGGA	NCBI36
NG_009244.1:g.130362_130366delinsGGGGA
NG_009244.2:g.130362_130366delinsGGGGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305877.13:c.3013-3698_3013-3694delinsGGGGA MANE Select	ENSP00000303507.8:n.3013-3698_3013-3694delinsGGGGA
ENST00000305877.12:c.3013-3698_3013-3694delinsGGGGA	ENSP00000303507.8:n.3013-3698_3013-3694delinsGGGGA
ENST00000359540.7:c.2881-3698_2881-3694delinsGGGGA	ENSP00000352535.3:n.2881-3698_2881-3694delinsGGGGA
ENST00000398512.9:c.1709-3698_1709-3694delinsGGGGA	ENSP00000381524.6:n.1709-3698_1709-3694delinsGGGGA
ENST00000419722.6:n.238-3698_238-3694delinsGGGGA
NM_004327.3:c.3013-3698_3013-3694delinsGGGGA	NP_004318.3:n.3013-3698_3013-3694delinsGGGGA
NM_021574.2:c.2881-3698_2881-3694delinsGGGGA	NP_067585.2:n.2881-3698_2881-3694delinsGGGGA
NM_004327.4:c.3013-3698_3013-3694delinsGGGGA MANE Select	NP_004318.3:n.3013-3698_3013-3694delinsGGGGA
NM_021574.3:c.2881-3698_2881-3694delinsGGGGA	NP_067585.2:n.2881-3698_2881-3694delinsGGGGA