Canonical Allele Identifier: CA500091389

Gene: CNTNAP1

Linked Data

• MyVariant Identifiers: chr17:g.40839959C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42687941C>T , CM000679.2:g.42687941C>T	GRCh38
NC_000017.10:g.40839959C>T , CM000679.1:g.40839959C>T	GRCh37
NC_000017.9:g.38093485C>T	NCBI36
NG_042091.1:g.10328C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264638.9:c.1266C>T MANE Select	ENSP00000264638.3:p.Ser422=
ENST00000264638.8:c.1266C>T	ENSP00000264638.3:p.Ser422=
ENST00000586801.1:n.681C>T
ENST00000591662.1:c.1266C>T	ENSP00000466571.1:p.Ser422=
NM_003632.2:c.1266C>T	NP_003623.1:p.Ser422=
XM_005257748.3:c.1038C>T	XP_005257805.1:p.Ser346=
XM_005257748.4:c.1038C>T	XP_005257805.1:p.Ser346=
XM_017025238.1:c.1266C>T	XP_016880727.1:p.Ser422=
XM_024451011.1:c.1266C>T	XP_024306779.1:p.Ser422=
NM_003632.3:c.1266C>T MANE Select	NP_003623.1:p.Ser422=