Canonical Allele Identifier: CA410896961

Gene: BCR

Linked Data

• MyVariant Identifiers: chr22:g.23627339C>A (hg19) ; chr22:g.23285152C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23285152C>A , CM000684.2:g.23285152C>A	GRCh38
NC_000022.10:g.23627339C>A , CM000684.1:g.23627339C>A	GRCh37
NC_000022.9:g.21957339C>A	NCBI36
NG_009244.1:g.109788C>A
NG_009244.2:g.109788C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305877.13:c.2357C>A MANE Select	ENSP00000303507.8:p.Ala786Asp
ENST00000305877.12:c.2357C>A	ENSP00000303507.8:p.Ala786Asp
ENST00000359540.7:c.2357C>A	ENSP00000352535.3:p.Ala786Asp
ENST00000398512.9:c.1270-2992C>A	ENSP00000381524.6:n.1270-2992C>A
ENST00000466076.1:n.431C>A
ENST00000487968.5:n.1010C>A
NM_004327.3:c.2357C>A	NP_004318.3:p.Ala786Asp
NM_021574.2:c.2357C>A	NP_067585.2:p.Ala786Asp
NM_004327.4:c.2357C>A MANE Select	NP_004318.3:p.Ala786Asp
NM_021574.3:c.2357C>A	NP_067585.2:p.Ala786Asp