Canonical Allele Identifier: CA2655647373
Gene: BCR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23285198_23285199del , CM000684.2:g.23285198_23285199del GRCh38
NC_000022.10:g.23627385_23627386del , CM000684.1:g.23627385_23627386del GRCh37
NC_000022.9:g.21957385_21957386del NCBI36
NG_009244.1:g.109834_109835del
NG_009244.2:g.109834_109835del

Transcript Alleles

HGVS Amino-acid change
ENST00000305877.13:c.2403_2404del MANE Select ENSP00000303507.8:p.Lys802GlufsTer?
ENST00000305877.12:c.2403_2404del ENSP00000303507.8:p.Lys802GlufsTer?
ENST00000359540.7:c.2403_2404del ENSP00000352535.3:p.Lys802GlufsTer?
ENST00000398512.9:c.1270-2946_1270-2945del ENSP00000381524.6:n.1270-2946_1270-2945de...
ENST00000466076.1:n.477_478del
ENST00000487968.5:n.1056_1057del
NM_004327.3:c.2403_2404del NP_004318.3:p.Lys802GlufsTer?
NM_021574.2:c.2403_2404del NP_067585.2:p.Lys802GlufsTer?
NM_004327.4:c.2403_2404del MANE Select NP_004318.3:p.Lys802GlufsTer?
NM_021574.3:c.2403_2404del NP_067585.2:p.Lys802GlufsTer?