Canonical Allele Identifier: CA410896829

Gene: BCR

Linked Data

• MyVariant Identifiers: chr22:g.23627297C>T (hg19) ; chr22:g.23285110C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23285110C>T , CM000684.2:g.23285110C>T	GRCh38
NC_000022.10:g.23627297C>T , CM000684.1:g.23627297C>T	GRCh37
NC_000022.9:g.21957297C>T	NCBI36
NG_009244.1:g.109746C>T
NG_009244.2:g.109746C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305877.13:c.2315C>T MANE Select	ENSP00000303507.8:p.Ala772Val
ENST00000305877.12:c.2315C>T	ENSP00000303507.8:p.Ala772Val
ENST00000359540.7:c.2315C>T	ENSP00000352535.3:p.Ala772Val
ENST00000398512.9:c.1270-3034C>T	ENSP00000381524.6:n.1270-3034C>T
ENST00000427791.1:c.767C>T	ENSP00000396531.1:p.Ala256Val
ENST00000466076.1:n.389C>T
ENST00000487968.5:n.968C>T
NM_004327.3:c.2315C>T	NP_004318.3:p.Ala772Val
NM_021574.2:c.2315C>T	NP_067585.2:p.Ala772Val
NM_004327.4:c.2315C>T MANE Select	NP_004318.3:p.Ala772Val
NM_021574.3:c.2315C>T	NP_067585.2:p.Ala772Val