Canonical Allele Identifier: CA1390688356

Gene: ALCAM

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.105541676C= , CM000665.2:g.105541676C=	GRCh38
NC_000003.11:g.105260520C= , CM000665.1:g.105260520C=	GRCh37
NC_000003.10:g.106743210C=	NCBI36
NG_029729.1:g.179964C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001627.4:c.902C= MANE Select	NP_001618.2:p.Thr301=
ENST00000306107.9:c.902C= MANE Select	ENSP00000305988.5:p.Thr301=
NM_001243280.1:c.902C=	NP_001230209.1:p.Thr301=
NM_001243280.2:c.902C=	NP_001230209.1:p.Thr301=
NM_001243281.1:c.902C=	NP_001230210.1:p.Thr301=
NM_001243281.2:c.902C=	NP_001230210.1:p.Thr301=
NM_001627.3:c.902C=	NP_001618.2:p.Thr301=
ENST00000465413.6:c.273-3547C=
ENST00000472644.6:c.902C=	ENSP00000419236.2:p.Thr301=
ENST00000481337.5:n.1031C=
ENST00000486979.6:c.749C=	ENSP00000418213.2:p.Thr250=