Canonical Allele Identifier: CA2002019782

Gene: CADM1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.115269862G= , CM000673.2:g.115269862G=	GRCh38
NC_000011.9:g.115140582G= , CM000673.1:g.115140582G=	GRCh37
NC_000011.8:g.114645792G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331581.11:c.125-29442C= MANE Select	ENSP00000329797.6:n.125-29442C=
ENST00000331581.10:c.125-29442C=	ENSP00000329797.6:n.125-29442C=
ENST00000452722.7:c.125-29442C=	ENSP00000395359.2:n.125-29442C=
ENST00000536727.5:c.125-29442C=	ENSP00000440322.1:n.125-29442C=
ENST00000537058.5:c.125-29442C=	ENSP00000439817.1:n.125-29442C=
ENST00000537140.5:n.254-29442C=
ENST00000540951.1:c.201-29442C=	ENSP00000445375.1:n.201-29442C=
ENST00000541434.5:n.125-29442C=
ENST00000542447.6:c.125-29442C=	ENSP00000439176.1:n.125-29442C=
ENST00000543249.1:c.76-29442C=
ENST00000543540.5:c.-318+17541C=	ENSP00000439847.1:n.-318+17541C=
ENST00000545380.5:c.120-29442C=
NM_001098517.1:c.125-29442C=	NP_001091987.1:n.125-29442C=
NM_001301043.1:c.125-29442C=	NP_001287972.1:n.125-29442C=
NM_001301044.1:c.125-29442C=	NP_001287973.1:n.125-29442C=
NM_001301045.1:c.125-29442C=	NP_001287974.1:n.125-29442C=
NM_014333.3:c.125-29442C=	NP_055148.3:n.125-29442C=
XM_005271494.2:c.125-29442C=	XP_005271551.1:n.125-29442C=
XM_005271494.3:c.125-29442C=	XP_005271551.1:n.125-29442C=
NM_001098517.2:c.125-29442C=	NP_001091987.1:n.125-29442C=
NM_001301043.2:c.125-29442C= MANE Select	NP_001287972.1:n.125-29442C=
NM_001301044.2:c.125-29442C=	NP_001287973.1:n.125-29442C=
NM_001301045.2:c.125-29442C=	NP_001287974.1:n.125-29442C=
NM_014333.4:c.125-29442C=	NP_055148.3:n.125-29442C=