Canonical Allele Identifier: CA399638079
Gene: CNTNAP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42687879C>A , CM000679.2:g.42687879C>A GRCh38
NC_000017.10:g.40839897C>A , CM000679.1:g.40839897C>A GRCh37
NC_000017.9:g.38093423C>A NCBI36
NG_042091.1:g.10266C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264638.9:c.1204C>A MANE Select ENSP00000264638.3:p.Arg402Ser
ENST00000264638.8:c.1204C>A ENSP00000264638.3:p.Arg402Ser
ENST00000586801.1:n.619C>A
ENST00000591662.1:c.1204C>A ENSP00000466571.1:p.Arg402Ser
NM_003632.2:c.1204C>A NP_003623.1:p.Arg402Ser
XM_005257748.3:c.976C>A XP_005257805.1:p.Arg326Ser
XM_005257748.4:c.976C>A XP_005257805.1:p.Arg326Ser
XM_017025238.1:c.1204C>A XP_016880727.1:p.Arg402Ser
XM_024451011.1:c.1204C>A XP_024306779.1:p.Arg402Ser
NM_003632.3:c.1204C>A MANE Select NP_003623.1:p.Arg402Ser