Canonical Allele Identifier: CA1375227678
Gene: CNTN3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.74578552T= , CM000665.2:g.74578552T= GRCh38
NC_000003.11:g.74627703T= , CM000665.1:g.74627703T= GRCh37
NC_000003.10:g.74710393T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000263665.7:c.-81+35839A= MANE Select ENSP00000263665.6:n.-81+35839A=
XM_005264757.2:c.-81+35839A= XP_005264814.1:n.-81+35839A=
XM_005264758.2:c.-81+35839A= XP_005264815.1:n.-81+35839A=
XM_005264757.3:c.-81+35839A= XP_005264814.1:n.-81+35839A=
XM_017006507.1:c.-81+35196A= XP_016861996.1:n.-81+35196A=
NM_001393376.1:c.-81+35196A= NP_001380305.1:n.-81+35196A=
NM_020872.3:c.-81+35839A= MANE Select NP_065923.1:n.-81+35839A=
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