Canonical Allele Identifier: CA1750229667
Gene: CNTNAP2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.146351655G= , CM000669.2:g.146351655G= GRCh38
NC_000007.13:g.146048747G= , CM000669.1:g.146048747G= GRCh37
NC_000007.12:g.145679680G= NCBI36
NG_007092.2:g.240295G=
NG_007092.3:g.240655G=

Transcript Alleles

HGVS Amino-acid change
ENST00000361727.8:c.97+234682G= MANE Select ENSP00000354778.3:n.97+234682G=
ENST00000637150.1:n.26+234682G=
ENST00000361727.7:c.97+234682G= ENSP00000354778.3:n.97+234682G=
ENST00000625365.2:c.97+234682G= ENSP00000485955.1:n.97+234682G=
NM_014141.5:c.97+234682G= NP_054860.1:n.97+234682G=
XM_017011950.2:c.97+234682G= XP_016867439.1:n.97+234682G=
NM_014141.6:c.97+234682G= MANE Select NP_054860.1:n.97+234682G=
Search 100 bp 5'
Search 100 bp 3'