Canonical Allele Identifier: CA2818514562

Gene: BCR

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23308993_23308994del , CM000684.2:g.23308993_23308994del	GRCh38
NC_000022.10:g.23651180_23651181del , CM000684.1:g.23651180_23651181del	GRCh37
NC_000022.9:g.21981180_21981181del	NCBI36
NG_009244.1:g.133629_133630del
NG_009244.2:g.133629_133630del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305877.13:c.3013-431_3013-430del MANE Select	ENSP00000303507.8:n.3013-431_3013-430del
ENST00000305877.12:c.3013-431_3013-430del	ENSP00000303507.8:n.3013-431_3013-430del
ENST00000359540.7:c.2881-431_2881-430del	ENSP00000352535.3:n.2881-431_2881-430del
ENST00000398512.9:c.1709-431_1709-430del	ENSP00000381524.6:n.1709-431_1709-430del
ENST00000419722.6:n.238-431_238-430del
ENST00000475025.5:n.87-431_87-430del
ENST00000478978.5:n.294-431_294-430del
NM_004327.3:c.3013-431_3013-430del	NP_004318.3:n.3013-431_3013-430del
NM_021574.2:c.2881-431_2881-430del	NP_067585.2:n.2881-431_2881-430del
NM_004327.4:c.3013-431_3013-430del MANE Select	NP_004318.3:n.3013-431_3013-430del
NM_021574.3:c.2881-431_2881-430del	NP_067585.2:n.2881-431_2881-430del