Canonical Allele Identifier: CA399637956
Gene: CNTNAP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42687846A>T , CM000679.2:g.42687846A>T GRCh38
NC_000017.10:g.40839864A>T , CM000679.1:g.40839864A>T GRCh37
NC_000017.9:g.38093390A>T NCBI36
NG_042091.1:g.10233A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264638.9:c.1171A>T MANE Select ENSP00000264638.3:p.Thr391Ser
ENST00000264638.8:c.1171A>T ENSP00000264638.3:p.Thr391Ser
ENST00000586801.1:n.586A>T
ENST00000591662.1:c.1171A>T ENSP00000466571.1:p.Thr391Ser
NM_003632.2:c.1171A>T NP_003623.1:p.Thr391Ser
XM_005257748.3:c.943A>T XP_005257805.1:p.Thr315Ser
XM_005257748.4:c.943A>T XP_005257805.1:p.Thr315Ser
XM_017025238.1:c.1171A>T XP_016880727.1:p.Thr391Ser
XM_024451011.1:c.1171A>T XP_024306779.1:p.Thr391Ser
NM_003632.3:c.1171A>T MANE Select NP_003623.1:p.Thr391Ser