Canonical Allele Identifier: CA399638031
Gene: CNTNAP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42687864C>T , CM000679.2:g.42687864C>T GRCh38
NC_000017.10:g.40839882C>T , CM000679.1:g.40839882C>T GRCh37
NC_000017.9:g.38093408C>T NCBI36
NG_042091.1:g.10251C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264638.9:c.1189C>T MANE Select ENSP00000264638.3:p.Leu397Phe
ENST00000264638.8:c.1189C>T ENSP00000264638.3:p.Leu397Phe
ENST00000586801.1:n.604C>T
ENST00000591662.1:c.1189C>T ENSP00000466571.1:p.Leu397Phe
NM_003632.2:c.1189C>T NP_003623.1:p.Leu397Phe
XM_005257748.3:c.961C>T XP_005257805.1:p.Leu321Phe
XM_005257748.4:c.961C>T XP_005257805.1:p.Leu321Phe
XM_017025238.1:c.1189C>T XP_016880727.1:p.Leu397Phe
XM_024451011.1:c.1189C>T XP_024306779.1:p.Leu397Phe
NM_003632.3:c.1189C>T MANE Select NP_003623.1:p.Leu397Phe