Canonical Allele Identifier: CA500091288
Gene: CNTNAP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.40839863C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42687845C>T , CM000679.2:g.42687845C>T GRCh38
NC_000017.10:g.40839863C>T , CM000679.1:g.40839863C>T GRCh37
NC_000017.9:g.38093389C>T NCBI36
NG_042091.1:g.10232C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000264638.9:c.1170C>T MANE Select ENSP00000264638.3:p.Arg390=
ENST00000264638.8:c.1170C>T ENSP00000264638.3:p.Arg390=
ENST00000586801.1:n.585C>T
ENST00000591662.1:c.1170C>T ENSP00000466571.1:p.Arg390=
NM_003632.2:c.1170C>T NP_003623.1:p.Arg390=
XM_005257748.3:c.942C>T XP_005257805.1:p.Arg314=
XM_005257748.4:c.942C>T XP_005257805.1:p.Arg314=
XM_017025238.1:c.1170C>T XP_016880727.1:p.Arg390=
XM_024451011.1:c.1170C>T XP_024306779.1:p.Arg390=
NM_003632.3:c.1170C>T MANE Select NP_003623.1:p.Arg390=