Canonical Allele Identifier: CA399637965
Gene: CNTNAP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42687849T>A , CM000679.2:g.42687849T>A GRCh38
NC_000017.10:g.40839867T>A , CM000679.1:g.40839867T>A GRCh37
NC_000017.9:g.38093393T>A NCBI36
NG_042091.1:g.10236T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000264638.9:c.1174T>A MANE Select ENSP00000264638.3:p.Trp392Arg
ENST00000264638.8:c.1174T>A ENSP00000264638.3:p.Trp392Arg
ENST00000586801.1:n.589T>A
ENST00000591662.1:c.1174T>A ENSP00000466571.1:p.Trp392Arg
NM_003632.2:c.1174T>A NP_003623.1:p.Trp392Arg
XM_005257748.3:c.946T>A XP_005257805.1:p.Trp316Arg
XM_005257748.4:c.946T>A XP_005257805.1:p.Trp316Arg
XM_017025238.1:c.1174T>A XP_016880727.1:p.Trp392Arg
XM_024451011.1:c.1174T>A XP_024306779.1:p.Trp392Arg
NM_003632.3:c.1174T>A MANE Select NP_003623.1:p.Trp392Arg