Canonical Allele Identifier: CA15687466

Gene: CADM1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.115226236A>T , CM000673.2:g.115226236A>T	GRCh38
NC_000011.9:g.115096956A>T , CM000673.1:g.115096956A>T	GRCh37
NC_000011.8:g.114602166A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331581.11:c.721+2877T>A MANE Select	ENSP00000329797.6:n.721+2877T>A
ENST00000331581.10:c.721+2877T>A	ENSP00000329797.6:n.721+2877T>A
ENST00000452722.7:c.721+2877T>A	ENSP00000395359.2:n.721+2877T>A
ENST00000536727.5:c.721+2877T>A	ENSP00000440322.1:n.721+2877T>A
ENST00000537058.5:c.721+2877T>A	ENSP00000439817.1:n.721+2877T>A
ENST00000537140.5:n.850+2877T>A
ENST00000541434.5:n.721+2877T>A
ENST00000542447.6:c.721+2877T>A	ENSP00000439176.1:n.721+2877T>A
ENST00000542450.5:c.280+2877T>A	ENSP00000442001.1:n.280+2877T>A
ENST00000545380.5:c.716+2877T>A
ENST00000612235.4:c.598+2877T>A	ENSP00000483648.1:n.598+2877T>A
ENST00000612471.4:c.598+2877T>A	ENSP00000483793.1:n.598+2877T>A
ENST00000616271.4:c.598+2877T>A	ENSP00000484516.1:n.598+2877T>A
ENST00000621043.4:c.598+2877T>A	ENSP00000482840.1:n.598+2877T>A
ENST00000621709.4:c.598+2877T>A	ENSP00000482924.1:n.598+2877T>A
NM_001098517.1:c.721+2877T>A	NP_001091987.1:n.721+2877T>A
NM_001301043.1:c.721+2877T>A	NP_001287972.1:n.721+2877T>A
NM_001301044.1:c.721+2877T>A	NP_001287973.1:n.721+2877T>A
NM_001301045.1:c.721+2877T>A	NP_001287974.1:n.721+2877T>A
NM_014333.3:c.721+2877T>A	NP_055148.3:n.721+2877T>A
XM_005271494.2:c.721+2877T>A	XP_005271551.1:n.721+2877T>A
XM_005271494.3:c.721+2877T>A	XP_005271551.1:n.721+2877T>A
XM_017017457.2:c.739+2877T>A	XP_016872946.1:n.739+2877T>A
NM_001098517.2:c.721+2877T>A	NP_001091987.1:n.721+2877T>A
NM_001301043.2:c.721+2877T>A MANE Select	NP_001287972.1:n.721+2877T>A
NM_001301044.2:c.721+2877T>A	NP_001287973.1:n.721+2877T>A
NM_001301045.2:c.721+2877T>A	NP_001287974.1:n.721+2877T>A
NM_014333.4:c.721+2877T>A	NP_055148.3:n.721+2877T>A