Canonical Allele Identifier: CA2397680717

Gene: BCR

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23216312_23216314delinsCAG , CM000684.2:g.23216312_23216314delinsCAG	GRCh38
NC_000022.10:g.23558499_23558501delinsCAG , CM000684.1:g.23558499_23558501delinsCAG	GRCh37
NC_000022.9:g.21888499_21888501delinsCAG	NCBI36
NG_009244.1:g.40948_40950delinsCAG
NG_009244.2:g.40948_40950delinsCAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000305877.13:c.1279+34073_1279+34075delinsCAG MANE Select	ENSP00000303507.8:n.1279+34073_1279+34075delinsCAG
ENST00000305877.12:c.1279+34073_1279+34075delinsCAG	ENSP00000303507.8:n.1279+34073_1279+34075delinsCAG
ENST00000359540.7:c.1279+34073_1279+34075delinsCAG	ENSP00000352535.3:n.1279+34073_1279+34075delinsCAG
ENST00000398512.9:c.1269+34083_1269+34085delinsCAG	ENSP00000381524.6:n.1269+34083_1269+34085delinsCAG
ENST00000463770.5:n.133+17927_133+17929delinsCAG
ENST00000479188.5:n.130-26506_130-26504delinsCAG
ENST00000487679.1:n.196+16960_196+16962delinsCAG
NM_004327.3:c.1279+34073_1279+34075delinsCAG	NP_004318.3:n.1279+34073_1279+34075delinsCAG
NM_021574.2:c.1279+34073_1279+34075delinsCAG	NP_067585.2:n.1279+34073_1279+34075delinsCAG
NM_004327.4:c.1279+34073_1279+34075delinsCAG MANE Select	NP_004318.3:n.1279+34073_1279+34075delinsCAG
NM_021574.3:c.1279+34073_1279+34075delinsCAG	NP_067585.2:n.1279+34073_1279+34075delinsCAG