Canonical Allele Identifier: CA369924669
Gene: CNTNAP2 HGNC NCBI

Linked Data

COSMIC: COSM254620

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.147132348C>T , CM000669.2:g.147132348C>T GRCh38
NC_000007.13:g.146829440C>T , CM000669.1:g.146829440C>T GRCh37
NC_000007.12:g.146460373C>T NCBI36
NG_007092.2:g.1020988C>T
NG_007092.3:g.1021348C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000361727.8:c.1187C>T MANE Select ENSP00000354778.3:p.Ser396Leu
ENST00000636561.1:n.1090C>T
ENST00000636870.1:n.1049C>T
ENST00000637150.1:n.1116C>T
ENST00000637694.1:n.1090C>T
ENST00000637825.1:n.670C>T
ENST00000638117.1:n.1090C>T
ENST00000361727.7:c.1187C>T ENSP00000354778.3:p.Ser396Leu
NM_014141.5:c.1187C>T NP_054860.1:p.Ser396Leu
XM_017011950.2:c.1187C>T XP_016867439.1:p.Ser396Leu
NM_014141.6:c.1187C>T MANE Select NP_054860.1:p.Ser396Leu