Canonical Allele Identifier: CA2002085342

Gene: CADM1

Linked Data

• dbSNP Id: rs1947458406

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.115411488G>A , CM000673.2:g.115411488G>A	GRCh38
NC_000011.9:g.115282206G>A , CM000673.1:g.115282206G>A	GRCh37
NC_000011.8:g.114787416G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000331581.11:c.124+92783C>T MANE Select	ENSP00000329797.6:n.124+92783C>T
ENST00000331581.10:c.124+92783C>T	ENSP00000329797.6:n.124+92783C>T
ENST00000452722.7:c.124+92783C>T	ENSP00000395359.2:n.124+92783C>T
ENST00000536727.5:c.124+92783C>T	ENSP00000440322.1:n.124+92783C>T
ENST00000536781.1:n.146-11975C>T
ENST00000537058.5:c.124+92783C>T	ENSP00000439817.1:n.124+92783C>T
ENST00000537140.5:n.253+92783C>T
ENST00000540951.1:c.200+34273C>T	ENSP00000445375.1:n.200+34273C>T
ENST00000541434.5:n.124+92783C>T
ENST00000542447.6:c.124+92783C>T	ENSP00000439176.1:n.124+92783C>T
ENST00000543249.1:c.75+93395C>T
ENST00000545380.5:c.119+92783C>T
NM_001098517.1:c.124+92783C>T	NP_001091987.1:n.124+92783C>T
NM_001301043.1:c.124+92783C>T	NP_001287972.1:n.124+92783C>T
NM_001301044.1:c.124+92783C>T	NP_001287973.1:n.124+92783C>T
NM_001301045.1:c.124+92783C>T	NP_001287974.1:n.124+92783C>T
NM_014333.3:c.124+92783C>T	NP_055148.3:n.124+92783C>T
XM_005271494.2:c.124+92783C>T	XP_005271551.1:n.124+92783C>T
XM_005271494.3:c.124+92783C>T	XP_005271551.1:n.124+92783C>T
NM_001098517.2:c.124+92783C>T	NP_001091987.1:n.124+92783C>T
NM_001301043.2:c.124+92783C>T MANE Select	NP_001287972.1:n.124+92783C>T
NM_001301044.2:c.124+92783C>T	NP_001287973.1:n.124+92783C>T
NM_001301045.2:c.124+92783C>T	NP_001287974.1:n.124+92783C>T
NM_014333.4:c.124+92783C>T	NP_055148.3:n.124+92783C>T