Canonical Allele Identifier: CA114290

Gene: BCAM

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44813547C>A , CM000681.2:g.44813547C>A	GRCh38
NC_000019.9:g.45316804C>A , CM000681.1:g.45316804C>A	GRCh37
NC_000019.8:g.50008644C>A	NCBI36
NG_007480.1:g.9467C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270233.12:c.711C>A MANE Select	ENSP00000270233.5:p.Cys237Ter
ENST00000591520.6:c.648C>A	ENSP00000467100.2:p.Cys216Ter
ENST00000611077.5:c.711C>A	ENSP00000481153.1:p.Cys237Ter
ENST00000270233.10:c.711C>A	ENSP00000270233.5:p.Cys237Ter
ENST00000589651.5:c.711C>A	ENSP00000476710.1:p.Cys237Ter
ENST00000590108.1:n.309C>A
ENST00000590196.1:c.110C>A
ENST00000591520.5:c.648C>A	ENSP00000467100.1:p.Cys216Ter
ENST00000611077.4:c.711C>A	ENSP00000481153.1:p.Cys237Ter
NM_001013257.2:c.711C>A	NP_001013275.1:p.Cys237Ter
NM_005581.4:c.711C>A	NP_005572.2:p.Cys237Ter
NM_005581.5:c.711C>A MANE Select	NP_005572.2:p.Cys237Ter