Canonical Allele Identifier: CA2002085335

Gene: CADM1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.115411473A= , CM000673.2:g.115411473A=	GRCh38
NC_000011.9:g.115282191A= , CM000673.1:g.115282191A=	GRCh37
NC_000011.8:g.114787401A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000331581.11:c.124+92798T= MANE Select	ENSP00000329797.6:n.124+92798T=
ENST00000331581.10:c.124+92798T=	ENSP00000329797.6:n.124+92798T=
ENST00000452722.7:c.124+92798T=	ENSP00000395359.2:n.124+92798T=
ENST00000536727.5:c.124+92798T=	ENSP00000440322.1:n.124+92798T=
ENST00000536781.1:n.146-11960T=
ENST00000537058.5:c.124+92798T=	ENSP00000439817.1:n.124+92798T=
ENST00000537140.5:n.253+92798T=
ENST00000540951.1:c.200+34288T=	ENSP00000445375.1:n.200+34288T=
ENST00000541434.5:n.124+92798T=
ENST00000542447.6:c.124+92798T=	ENSP00000439176.1:n.124+92798T=
ENST00000543249.1:c.75+93410T=
ENST00000545380.5:c.119+92798T=
NM_001098517.1:c.124+92798T=	NP_001091987.1:n.124+92798T=
NM_001301043.1:c.124+92798T=	NP_001287972.1:n.124+92798T=
NM_001301044.1:c.124+92798T=	NP_001287973.1:n.124+92798T=
NM_001301045.1:c.124+92798T=	NP_001287974.1:n.124+92798T=
NM_014333.3:c.124+92798T=	NP_055148.3:n.124+92798T=
XM_005271494.2:c.124+92798T=	XP_005271551.1:n.124+92798T=
XM_005271494.3:c.124+92798T=	XP_005271551.1:n.124+92798T=
NM_001098517.2:c.124+92798T=	NP_001091987.1:n.124+92798T=
NM_001301043.2:c.124+92798T= MANE Select	NP_001287972.1:n.124+92798T=
NM_001301044.2:c.124+92798T=	NP_001287973.1:n.124+92798T=
NM_001301045.2:c.124+92798T=	NP_001287974.1:n.124+92798T=
NM_014333.4:c.124+92798T=	NP_055148.3:n.124+92798T=