Canonical Allele Identifier: CA2818511585

Gene: BCR

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23203793_23203795del , CM000684.2:g.23203793_23203795del	GRCh38
NC_000022.10:g.23545980_23545982del , CM000684.1:g.23545980_23545982del	GRCh37
NC_000022.9:g.21875980_21875982del	NCBI36
NG_009244.1:g.28429_28431del
NG_009244.2:g.28429_28431del

Transcript Alleles

HGVS	Amino-acid change
ENST00000305877.13:c.1279+21554_1279+21556del MANE Select	ENSP00000303507.8:n.1279+21554_1279+21556del
ENST00000305877.12:c.1279+21554_1279+21556del	ENSP00000303507.8:n.1279+21554_1279+21556del
ENST00000359540.7:c.1279+21554_1279+21556del	ENSP00000352535.3:n.1279+21554_1279+21556del
ENST00000398512.9:c.1269+21564_1269+21566del	ENSP00000381524.6:n.1269+21564_1269+21566del
ENST00000463770.5:n.133+5408_133+5410del
ENST00000479188.5:n.129+23961_129+23963del
ENST00000487679.1:n.196+4441_196+4443del
NM_004327.3:c.1279+21554_1279+21556del	NP_004318.3:n.1279+21554_1279+21556del
NM_021574.2:c.1279+21554_1279+21556del	NP_067585.2:n.1279+21554_1279+21556del
NM_004327.4:c.1279+21554_1279+21556del MANE Select	NP_004318.3:n.1279+21554_1279+21556del
NM_021574.3:c.1279+21554_1279+21556del	NP_067585.2:n.1279+21554_1279+21556del