Canonical Allele Identifier: CA2338120335
Gene: BCAM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44812233T= , CM000681.2:g.44812233T= GRCh38
NC_000019.9:g.45315490T= , CM000681.1:g.45315490T= GRCh37
NC_000019.8:g.50007330T= NCBI36
NG_007480.1:g.8153T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000270233.12:c.275T= MANE Select ENSP00000270233.5:p.Met92=
ENST00000591520.6:c.212T= ENSP00000467100.2:p.Met71=
ENST00000611077.5:c.275T= ENSP00000481153.1:p.Met92=
ENST00000270233.10:c.275T= ENSP00000270233.5:p.Met92=
ENST00000588603.1:n.270T=
ENST00000589651.5:c.275T= ENSP00000476710.1:p.Met92=
ENST00000591520.5:c.212T= ENSP00000467100.1:p.Met71=
ENST00000611077.4:c.275T= ENSP00000481153.1:p.Met92=
NM_001013257.2:c.275T= NP_001013275.1:p.Met92=
NM_005581.4:c.275T= NP_005572.2:p.Met92=
NM_005581.5:c.275T= MANE Select NP_005572.2:p.Met92=