Canonical Allele Identifier: CA2397726846

Gene: BCR

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23308738_23308740delinsCAT , CM000684.2:g.23308738_23308740delinsCAT	GRCh38
NC_000022.10:g.23650925_23650927delinsCAT , CM000684.1:g.23650925_23650927delinsCAT	GRCh37
NC_000022.9:g.21980925_21980927delinsCAT	NCBI36
NG_009244.1:g.133374_133376delinsCAT
NG_009244.2:g.133374_133376delinsCAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305877.13:c.3013-686_3013-684delinsCAT MANE Select	ENSP00000303507.8:n.3013-686_3013-684delinsCAT
ENST00000305877.12:c.3013-686_3013-684delinsCAT	ENSP00000303507.8:n.3013-686_3013-684delinsCAT
ENST00000359540.7:c.2881-686_2881-684delinsCAT	ENSP00000352535.3:n.2881-686_2881-684delinsCAT
ENST00000398512.9:c.1709-686_1709-684delinsCAT	ENSP00000381524.6:n.1709-686_1709-684delinsCAT
ENST00000419722.6:n.238-686_238-684delinsCAT
ENST00000475025.5:n.87-686_87-684delinsCAT
ENST00000478978.5:n.294-686_294-684delinsCAT
NM_004327.3:c.3013-686_3013-684delinsCAT	NP_004318.3:n.3013-686_3013-684delinsCAT
NM_021574.2:c.2881-686_2881-684delinsCAT	NP_067585.2:n.2881-686_2881-684delinsCAT
NM_004327.4:c.3013-686_3013-684delinsCAT MANE Select	NP_004318.3:n.3013-686_3013-684delinsCAT
NM_021574.3:c.2881-686_2881-684delinsCAT	NP_067585.2:n.2881-686_2881-684delinsCAT