Canonical Allele Identifier: CA1375227633
Gene: CNTN3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.74578453T= , CM000665.2:g.74578453T= GRCh38
NC_000003.11:g.74627604T= , CM000665.1:g.74627604T= GRCh37
NC_000003.10:g.74710294T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000263665.7:c.-81+35938A= MANE Select ENSP00000263665.6:n.-81+35938A=
XM_005264757.2:c.-81+35938A= XP_005264814.1:n.-81+35938A=
XM_005264758.2:c.-81+35938A= XP_005264815.1:n.-81+35938A=
XM_005264757.3:c.-81+35938A= XP_005264814.1:n.-81+35938A=
XM_017006507.1:c.-81+35295A= XP_016861996.1:n.-81+35295A=
NM_001393376.1:c.-81+35295A= NP_001380305.1:n.-81+35295A=
NM_020872.3:c.-81+35938A= MANE Select NP_065923.1:n.-81+35938A=