Canonical Allele Identifier: CA1750654834
Gene: CNTNAP2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.147200268G= , CM000669.2:g.147200268G= GRCh38
NC_000007.13:g.146897360G= , CM000669.1:g.146897360G= GRCh37
NC_000007.12:g.146528293G= NCBI36
NG_007092.2:g.1088908G=
NG_007092.3:g.1089268G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361727.8:c.1348+67759G= MANE Select ENSP00000354778.3:n.1348+67759G=
ENST00000636870.1:n.1210+67759G=
ENST00000637694.1:n.1251+67759G=
ENST00000637825.1:n.831+67759G=
ENST00000638117.1:n.1251+67759G=
ENST00000361727.7:c.1348+67759G= ENSP00000354778.3:n.1348+67759G=
NM_014141.5:c.1348+67759G= NP_054860.1:n.1348+67759G=
XM_017011950.2:c.1348+67759G= XP_016867439.1:n.1348+67759G=
NM_014141.6:c.1348+67759G= MANE Select NP_054860.1:n.1348+67759G=
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