Canonical Allele Identifier: CA1380685972

Gene: CADM2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.85555773C= , CM000665.2:g.85555773C=	GRCh38
NC_000003.11:g.85604923C= , CM000665.1:g.85604923C=	GRCh37
NC_000003.10:g.85687613C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383699.8:c.62-170749C= MANE Select	ENSP00000373200.3:n.62-170749C=
ENST00000383699.7:c.62-170749C=	ENSP00000373200.3:n.62-170749C=
ENST00000407528.6:c.62-246274C=	ENSP00000384575.2:n.62-246274C=
NM_001167674.1:c.62-246274C=	NP_001161146.1:n.62-246274C=
NM_001167675.1:c.62-170749C=	NP_001161147.1:n.62-170749C=
NM_001256502.1:c.-264+43875C=	NP_001243431.1:n.-264+43875C=
NM_001256503.1:c.-114+43875C=	NP_001243432.1:n.-114+43875C=
NM_001256504.1:c.-291+43875C=	NP_001243433.1:n.-291+43875C=
NM_001256505.1:c.-264+43875C=	NP_001243434.1:n.-264+43875C=
XM_006713081.2:c.62-246274C=	XP_006713144.1:n.62-246274C=
XM_006713082.2:c.62-246274C=	XP_006713145.1:n.62-246274C=
XM_006713081.4:c.62-246274C=	XP_006713144.1:n.62-246274C=
XM_006713082.3:c.62-246274C=	XP_006713145.1:n.62-246274C=
XM_017006062.2:c.103+43875C=	XP_016861551.1:n.103+43875C=
NM_001167674.2:c.62-246274C=	NP_001161146.1:n.62-246274C=
NM_001167675.2:c.62-170749C= MANE Select	NP_001161147.1:n.62-170749C=
NM_001256502.2:c.-264+43875C=	NP_001243431.1:n.-264+43875C=
NM_001256503.2:c.-114+43875C=	NP_001243432.1:n.-114+43875C=
NM_001256504.2:c.-291+43875C=	NP_001243433.1:n.-291+43875C=
NM_001256505.2:c.-264+43875C=	NP_001243434.1:n.-264+43875C=
NM_001375960.1:c.62-170749C=	NP_001362889.1:n.62-170749C=
NM_001375961.1:c.-86-170749C=	NP_001362890.1:n.-86-170749C=
NM_001375964.1:c.62-170749C=	NP_001362893.1:n.62-170749C=
NM_001375967.1:c.62-170749C=	NP_001362896.1:n.62-170749C=
NM_001375968.1:c.62-170749C=	NP_001362897.1:n.62-170749C=
NM_001381963.1:c.62-246274C=	NP_001368892.1:n.62-246274C=
NM_001381964.1:c.62-246274C=	NP_001368893.1:n.62-246274C=