Canonical Allele Identifier: CA2397714795

Gene: BCR

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23285064_23285065delinsAT , CM000684.2:g.23285064_23285065delinsAT	GRCh38
NC_000022.10:g.23627251_23627252delinsAT , CM000684.1:g.23627251_23627252delinsAT	GRCh37
NC_000022.9:g.21957251_21957252delinsAT	NCBI36
NG_009244.1:g.109700_109701delinsAT
NG_009244.2:g.109700_109701delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305877.13:c.2269_2270delinsAT MANE Select	ENSP00000303507.8:p.Ile757=
ENST00000305877.12:c.2269_2270delinsAT	ENSP00000303507.8:p.Ile757=
ENST00000359540.7:c.2269_2270delinsAT	ENSP00000352535.3:p.Ile757=
ENST00000398512.9:c.1270-3080_1270-3079delinsAT	ENSP00000381524.6:n.1270-3080_1270-3079delinsAT
ENST00000427791.1:c.721_722delinsAT	ENSP00000396531.1:p.Ile241=
ENST00000466076.1:n.343_344delinsAT
ENST00000487968.5:n.922_923delinsAT
NM_004327.3:c.2269_2270delinsAT	NP_004318.3:p.Ile757=
NM_021574.2:c.2269_2270delinsAT	NP_067585.2:p.Ile757=
NM_004327.4:c.2269_2270delinsAT MANE Select	NP_004318.3:p.Ile757=
NM_021574.3:c.2269_2270delinsAT	NP_067585.2:p.Ile757=