Canonical Allele Identifier: CA369924807
Gene: CNTNAP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.147132412T>G , CM000669.2:g.147132412T>G GRCh38
NC_000007.13:g.146829504T>G , CM000669.1:g.146829504T>G GRCh37
NC_000007.12:g.146460437T>G NCBI36
NG_007092.2:g.1021052T>G
NG_007092.3:g.1021412T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000361727.8:c.1251T>G MANE Select ENSP00000354778.3:p.Asp417Glu
ENST00000636561.1:n.1154T>G
ENST00000636870.1:n.1113T>G
ENST00000637150.1:n.1180T>G
ENST00000637694.1:n.1154T>G
ENST00000637825.1:n.734T>G
ENST00000638117.1:n.1154T>G
ENST00000361727.7:c.1251T>G ENSP00000354778.3:p.Asp417Glu
NM_014141.5:c.1251T>G NP_054860.1:p.Asp417Glu
XM_017011950.2:c.1251T>G XP_016867439.1:p.Asp417Glu
NM_014141.6:c.1251T>G MANE Select NP_054860.1:p.Asp417Glu