Canonical Allele Identifier: CA2818513862

Gene: BCR

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23285105_23285106insTCC , CM000684.2:g.23285105_23285106insTCC	GRCh38
NC_000022.10:g.23627292_23627293insTCC , CM000684.1:g.23627292_23627293insTCC	GRCh37
NC_000022.9:g.21957292_21957293insTCC	NCBI36
NG_009244.1:g.109741_109742insTCC
NG_009244.2:g.109741_109742insTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305877.13:c.2310_2311insTCC MANE Select	ENSP00000303507.8:p.Leu770_Glu771insSer
ENST00000305877.12:c.2310_2311insTCC	ENSP00000303507.8:p.Leu770_Glu771insSer
ENST00000359540.7:c.2310_2311insTCC	ENSP00000352535.3:p.Leu770_Glu771insSer
ENST00000398512.9:c.1270-3039_1270-3038insTCC	ENSP00000381524.6:n.1270-3039_1270-3038insTCC
ENST00000427791.1:c.762_763insTCC	ENSP00000396531.1:p.Leu254_Glu255insSer
ENST00000466076.1:n.384_385insTCC
ENST00000487968.5:n.963_964insTCC
NM_004327.3:c.2310_2311insTCC	NP_004318.3:p.Leu770_Glu771insSer
NM_021574.2:c.2310_2311insTCC	NP_067585.2:p.Leu770_Glu771insSer
NM_004327.4:c.2310_2311insTCC MANE Select	NP_004318.3:p.Leu770_Glu771insSer
NM_021574.3:c.2310_2311insTCC	NP_067585.2:p.Leu770_Glu771insSer