Canonical Allele Identifier: CA751769436

Gene: BCR

Linked Data

• dbSNP Id: rs1459867752
• gnomAD v3: 22-23308716-C-CA
• gnomAD v4: 22-23308716-C-CA
• MyVariant Identifiers: chr22:g.23650903_23650904insA (hg19) ; chr22:g.23308716_23308717insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23308717dup , CM000684.2:g.23308717dup	GRCh38
NC_000022.10:g.23650904dup , CM000684.1:g.23650904dup	GRCh37
NC_000022.9:g.21980904dup	NCBI36
NG_009244.1:g.133353dup
NG_009244.2:g.133353dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305877.13:c.3013-707dup MANE Select	ENSP00000303507.8:n.3013-707dup
ENST00000305877.12:c.3013-707dup	ENSP00000303507.8:n.3013-707dup
ENST00000359540.7:c.2881-707dup	ENSP00000352535.3:n.2881-707dup
ENST00000398512.9:c.1709-707dup	ENSP00000381524.6:n.1709-707dup
ENST00000419722.6:n.238-707dup
ENST00000475025.5:n.87-707dup
ENST00000478978.5:n.294-707dup
NM_004327.3:c.3013-707dup	NP_004318.3:n.3013-707dup
NM_021574.2:c.2881-707dup	NP_067585.2:n.2881-707dup
NM_004327.4:c.3013-707dup MANE Select	NP_004318.3:n.3013-707dup
NM_021574.3:c.2881-707dup	NP_067585.2:n.2881-707dup