Canonical Allele Identifier: CA2338120326
Gene: BCAM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44812219G= , CM000681.2:g.44812219G= GRCh38
NC_000019.9:g.45315476G= , CM000681.1:g.45315476G= GRCh37
NC_000019.8:g.50007316G= NCBI36
NG_007480.1:g.8139G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000270233.12:c.261G= MANE Select ENSP00000270233.5:p.Glu87=
ENST00000591520.6:c.205-7G= ENSP00000467100.2:n.205-7G=
ENST00000611077.5:c.261G= ENSP00000481153.1:p.Glu87=
ENST00000270233.10:c.261G= ENSP00000270233.5:p.Glu87=
ENST00000588603.1:n.256G=
ENST00000589651.5:c.261G= ENSP00000476710.1:p.Glu87=
ENST00000591520.5:c.205-7G= ENSP00000467100.1:n.205-7G=
ENST00000611077.4:c.261G= ENSP00000481153.1:p.Glu87=
NM_001013257.2:c.261G= NP_001013275.1:p.Glu87=
NM_005581.4:c.261G= NP_005572.2:p.Glu87=
NM_005581.5:c.261G= MANE Select NP_005572.2:p.Glu87=