Canonical Allele Identifier: CA507946177

Gene: BCAM

Linked Data

• MyVariant Identifiers: chr19:g.45315488A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44812231A>G , CM000681.2:g.44812231A>G	GRCh38
NC_000019.9:g.45315488A>G , CM000681.1:g.45315488A>G	GRCh37
NC_000019.8:g.50007328A>G	NCBI36
NG_007480.1:g.8151A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270233.12:c.273A>G MANE Select	ENSP00000270233.5:p.Thr91=
ENST00000591520.6:c.210A>G	ENSP00000467100.2:p.Thr70=
ENST00000611077.5:c.273A>G	ENSP00000481153.1:p.Thr91=
ENST00000270233.10:c.273A>G	ENSP00000270233.5:p.Thr91=
ENST00000588603.1:n.268A>G
ENST00000589651.5:c.273A>G	ENSP00000476710.1:p.Thr91=
ENST00000591520.5:c.210A>G	ENSP00000467100.1:p.Thr70=
ENST00000611077.4:c.273A>G	ENSP00000481153.1:p.Thr91=
NM_001013257.2:c.273A>G	NP_001013275.1:p.Thr91=
NM_005581.4:c.273A>G	NP_005572.2:p.Thr91=
NM_005581.5:c.273A>G MANE Select	NP_005572.2:p.Thr91=