Canonical Allele Identifier: CA2397674349

Gene: BCR

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23203666_23203667delinsTC , CM000684.2:g.23203666_23203667delinsTC	GRCh38
NC_000022.10:g.23545853_23545854delinsTC , CM000684.1:g.23545853_23545854delinsTC	GRCh37
NC_000022.9:g.21875853_21875854delinsTC	NCBI36
NG_009244.1:g.28302_28303delinsTC
NG_009244.2:g.28302_28303delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305877.13:c.1279+21427_1279+21428delinsTC MANE Select	ENSP00000303507.8:n.1279+21427_1279+21428delinsTC
ENST00000305877.12:c.1279+21427_1279+21428delinsTC	ENSP00000303507.8:n.1279+21427_1279+21428delinsTC
ENST00000359540.7:c.1279+21427_1279+21428delinsTC	ENSP00000352535.3:n.1279+21427_1279+21428delinsTC
ENST00000398512.9:c.1269+21437_1269+21438delinsTC	ENSP00000381524.6:n.1269+21437_1269+21438delinsTC
ENST00000463770.5:n.133+5281_133+5282delinsTC
ENST00000479188.5:n.129+23834_129+23835delinsTC
ENST00000487679.1:n.196+4314_196+4315delinsTC
NM_004327.3:c.1279+21427_1279+21428delinsTC	NP_004318.3:n.1279+21427_1279+21428delinsTC
NM_021574.2:c.1279+21427_1279+21428delinsTC	NP_067585.2:n.1279+21427_1279+21428delinsTC
NM_004327.4:c.1279+21427_1279+21428delinsTC MANE Select	NP_004318.3:n.1279+21427_1279+21428delinsTC
NM_021574.3:c.1279+21427_1279+21428delinsTC	NP_067585.2:n.1279+21427_1279+21428delinsTC