Canonical Allele Identifier: CA1375227679
Gene: CNTN3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.74578556A= , CM000665.2:g.74578556A= GRCh38
NC_000003.11:g.74627707A= , CM000665.1:g.74627707A= GRCh37
NC_000003.10:g.74710397A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000263665.7:c.-81+35835T= MANE Select ENSP00000263665.6:n.-81+35835T=
XM_005264757.2:c.-81+35835T= XP_005264814.1:n.-81+35835T=
XM_005264758.2:c.-81+35835T= XP_005264815.1:n.-81+35835T=
XM_005264757.3:c.-81+35835T= XP_005264814.1:n.-81+35835T=
XM_017006507.1:c.-81+35192T= XP_016861996.1:n.-81+35192T=
NM_001393376.1:c.-81+35192T= NP_001380305.1:n.-81+35192T=
NM_020872.3:c.-81+35835T= MANE Select NP_065923.1:n.-81+35835T=