Canonical Allele Identifier: CA399638311
Gene: CNTNAP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42687933A>G , CM000679.2:g.42687933A>G GRCh38
NC_000017.10:g.40839951A>G , CM000679.1:g.40839951A>G GRCh37
NC_000017.9:g.38093477A>G NCBI36
NG_042091.1:g.10320A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264638.9:c.1258A>G MANE Select ENSP00000264638.3:p.Asn420Asp
ENST00000264638.8:c.1258A>G ENSP00000264638.3:p.Asn420Asp
ENST00000586801.1:n.673A>G
ENST00000591662.1:c.1258A>G ENSP00000466571.1:p.Asn420Asp
NM_003632.2:c.1258A>G NP_003623.1:p.Asn420Asp
XM_005257748.3:c.1030A>G XP_005257805.1:p.Asn344Asp
XM_005257748.4:c.1030A>G XP_005257805.1:p.Asn344Asp
XM_017025238.1:c.1258A>G XP_016880727.1:p.Asn420Asp
XM_024451011.1:c.1258A>G XP_024306779.1:p.Asn420Asp
NM_003632.3:c.1258A>G MANE Select NP_003623.1:p.Asn420Asp