Canonical Allele Identifier: CA1024478602

Gene: BCR

Linked Data

• dbSNP Id: rs2073975452
• gnomAD v3: 22-23308755-A-ACAGT
• gnomAD v4: 22-23308755-A-ACAGT

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23308758_23308759insTCAG , CM000684.2:g.23308758_23308759insTCAG	GRCh38
NC_000022.10:g.23650945_23650946insTCAG , CM000684.1:g.23650945_23650946insTCAG	GRCh37
NC_000022.9:g.21980945_21980946insTCAG	NCBI36
NG_009244.1:g.133394_133395insTCAG
NG_009244.2:g.133394_133395insTCAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000305877.13:c.3013-666_3013-665insTCAG MANE Select	ENSP00000303507.8:n.3013-666_3013-665insTCAG
ENST00000305877.12:c.3013-666_3013-665insTCAG	ENSP00000303507.8:n.3013-666_3013-665insTCAG
ENST00000359540.7:c.2881-666_2881-665insTCAG	ENSP00000352535.3:n.2881-666_2881-665insTCAG
ENST00000398512.9:c.1709-666_1709-665insTCAG	ENSP00000381524.6:n.1709-666_1709-665insTCAG
ENST00000419722.6:n.238-666_238-665insTCAG
ENST00000475025.5:n.87-666_87-665insTCAG
ENST00000478978.5:n.294-666_294-665insTCAG
NM_004327.3:c.3013-666_3013-665insTCAG	NP_004318.3:n.3013-666_3013-665insTCAG
NM_021574.2:c.2881-666_2881-665insTCAG	NP_067585.2:n.2881-666_2881-665insTCAG
NM_004327.4:c.3013-666_3013-665insTCAG MANE Select	NP_004318.3:n.3013-666_3013-665insTCAG
NM_021574.3:c.2881-666_2881-665insTCAG	NP_067585.2:n.2881-666_2881-665insTCAG