Canonical Allele Identifier: CA1380639056
Gene: CADM2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.85469430A>C , CM000665.2:g.85469430A>C GRCh38
NC_000003.11:g.85518580A>C , CM000665.1:g.85518580A>C GRCh37
NC_000003.10:g.85601270A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000383699.8:c.62-257092A>C MANE Select ENSP00000373200.3:n.62-257092A>C
ENST00000383699.7:c.62-257092A>C ENSP00000373200.3:n.62-257092A>C
ENST00000407528.6:c.62-332617A>C ENSP00000384575.2:n.62-332617A>C
NM_001167674.1:c.62-332617A>C NP_001161146.1:n.62-332617A>C
NM_001167675.1:c.62-257092A>C NP_001161147.1:n.62-257092A>C
XM_006713081.2:c.62-332617A>C XP_006713144.1:n.62-332617A>C
XM_006713082.2:c.62-332617A>C XP_006713145.1:n.62-332617A>C
XM_006713081.4:c.62-332617A>C XP_006713144.1:n.62-332617A>C
XM_006713082.3:c.62-332617A>C XP_006713145.1:n.62-332617A>C
XM_017006062.2:c.62-42427A>C XP_016861551.1:n.62-42427A>C
NM_001167674.2:c.62-332617A>C NP_001161146.1:n.62-332617A>C
NM_001167675.2:c.62-257092A>C MANE Select NP_001161147.1:n.62-257092A>C
NM_001375960.1:c.62-257092A>C NP_001362889.1:n.62-257092A>C
NM_001375961.1:c.-86-257092A>C NP_001362890.1:n.-86-257092A>C
NM_001375964.1:c.62-257092A>C NP_001362893.1:n.62-257092A>C
NM_001375967.1:c.62-257092A>C NP_001362896.1:n.62-257092A>C
NM_001375968.1:c.62-257092A>C NP_001362897.1:n.62-257092A>C
NM_001381963.1:c.62-332617A>C NP_001368892.1:n.62-332617A>C
NM_001381964.1:c.62-332617A>C NP_001368893.1:n.62-332617A>C