Canonical Allele Identifier: CA1380631064
Gene: CADM2 HGNC NCBI

Linked Data

dbSNP Id: rs13323436

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.85453695T>C , CM000665.2:g.85453695T>C GRCh38
NC_000003.11:g.85502845T>C , CM000665.1:g.85502845T>C GRCh37
NC_000003.10:g.85585535T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000383699.8:c.62-272827T>C MANE Select ENSP00000373200.3:n.62-272827T>C
ENST00000383699.7:c.62-272827T>C ENSP00000373200.3:n.62-272827T>C
ENST00000407528.6:c.62-348352T>C ENSP00000384575.2:n.62-348352T>C
NM_001167674.1:c.62-348352T>C NP_001161146.1:n.62-348352T>C
NM_001167675.1:c.62-272827T>C NP_001161147.1:n.62-272827T>C
XM_006713081.2:c.62-348352T>C XP_006713144.1:n.62-348352T>C
XM_006713082.2:c.62-348352T>C XP_006713145.1:n.62-348352T>C
XM_006713081.4:c.62-348352T>C XP_006713144.1:n.62-348352T>C
XM_006713082.3:c.62-348352T>C XP_006713145.1:n.62-348352T>C
XM_017006062.2:c.62-58162T>C XP_016861551.1:n.62-58162T>C
NM_001167674.2:c.62-348352T>C NP_001161146.1:n.62-348352T>C
NM_001167675.2:c.62-272827T>C MANE Select NP_001161147.1:n.62-272827T>C
NM_001375960.1:c.62-272827T>C NP_001362889.1:n.62-272827T>C
NM_001375961.1:c.-86-272827T>C NP_001362890.1:n.-86-272827T>C
NM_001375964.1:c.62-272827T>C NP_001362893.1:n.62-272827T>C
NM_001375967.1:c.62-272827T>C NP_001362896.1:n.62-272827T>C
NM_001375968.1:c.62-272827T>C NP_001362897.1:n.62-272827T>C
NM_001381963.1:c.62-348352T>C NP_001368892.1:n.62-348352T>C
NM_001381964.1:c.62-348352T>C NP_001368893.1:n.62-348352T>C