Canonical Allele Identifier: CA751758753

Gene: BCR

Linked Data

• dbSNP Id: rs1369830153
• MyVariant Identifiers: chr22:g.23558591_23558592insT (hg19) ; chr22:g.23216404_23216405insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23216406dup , CM000684.2:g.23216406dup	GRCh38
NC_000022.10:g.23558593dup , CM000684.1:g.23558593dup	GRCh37
NC_000022.9:g.21888593dup	NCBI36
NG_009244.1:g.41042dup
NG_009244.2:g.41042dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305877.13:c.1279+34167dup MANE Select	ENSP00000303507.8:n.1279+34167dup
ENST00000305877.12:c.1279+34167dup	ENSP00000303507.8:n.1279+34167dup
ENST00000359540.7:c.1279+34167dup	ENSP00000352535.3:n.1279+34167dup
ENST00000398512.9:c.1269+34177dup	ENSP00000381524.6:n.1269+34177dup
ENST00000463770.5:n.133+18021dup
ENST00000479188.5:n.130-26412dup
ENST00000487679.1:n.196+17054dup
NM_004327.3:c.1279+34167dup	NP_004318.3:n.1279+34167dup
NM_021574.2:c.1279+34167dup	NP_067585.2:n.1279+34167dup
NM_004327.4:c.1279+34167dup MANE Select	NP_004318.3:n.1279+34167dup
NM_021574.3:c.1279+34167dup	NP_067585.2:n.1279+34167dup