Canonical Allele Identifier: CA1750654980
Gene: CNTNAP2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.147200597G= , CM000669.2:g.147200597G= GRCh38
NC_000007.13:g.146897689G= , CM000669.1:g.146897689G= GRCh37
NC_000007.12:g.146528622G= NCBI36
NG_007092.2:g.1089237G=
NG_007092.3:g.1089597G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361727.8:c.1348+68088G= MANE Select ENSP00000354778.3:n.1348+68088G=
ENST00000636870.1:n.1210+68088G=
ENST00000637694.1:n.1251+68088G=
ENST00000637825.1:n.831+68088G=
ENST00000638117.1:n.1251+68088G=
ENST00000361727.7:c.1348+68088G= ENSP00000354778.3:n.1348+68088G=
NM_014141.5:c.1348+68088G= NP_054860.1:n.1348+68088G=
XM_017011950.2:c.1348+68088G= XP_016867439.1:n.1348+68088G=
NM_014141.6:c.1348+68088G= MANE Select NP_054860.1:n.1348+68088G=
Search 100 bp 5'
Search 100 bp 3'