Canonical Allele Identifier: CA2397726775

Gene: BCR

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23308609_23308610delinsAG , CM000684.2:g.23308609_23308610delinsAG	GRCh38
NC_000022.10:g.23650796_23650797delinsAG , CM000684.1:g.23650796_23650797delinsAG	GRCh37
NC_000022.9:g.21980796_21980797delinsAG	NCBI36
NG_009244.1:g.133245_133246delinsAG
NG_009244.2:g.133245_133246delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305877.13:c.3013-815_3013-814delinsAG MANE Select	ENSP00000303507.8:n.3013-815_3013-814delinsAG
ENST00000305877.12:c.3013-815_3013-814delinsAG	ENSP00000303507.8:n.3013-815_3013-814delinsAG
ENST00000359540.7:c.2881-815_2881-814delinsAG	ENSP00000352535.3:n.2881-815_2881-814delinsAG
ENST00000398512.9:c.1709-815_1709-814delinsAG	ENSP00000381524.6:n.1709-815_1709-814delinsAG
ENST00000419722.6:n.238-815_238-814delinsAG
ENST00000475025.5:n.87-815_87-814delinsAG
ENST00000478978.5:n.294-815_294-814delinsAG
NM_004327.3:c.3013-815_3013-814delinsAG	NP_004318.3:n.3013-815_3013-814delinsAG
NM_021574.2:c.2881-815_2881-814delinsAG	NP_067585.2:n.2881-815_2881-814delinsAG
NM_004327.4:c.3013-815_3013-814delinsAG MANE Select	NP_004318.3:n.3013-815_3013-814delinsAG
NM_021574.3:c.2881-815_2881-814delinsAG	NP_067585.2:n.2881-815_2881-814delinsAG