Canonical Allele Identifier: CA1750443812
Gene: CNTNAP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.146792622_146792623delinsTA , CM000669.2:g.146792622_146792623delinsTA GRCh38
NC_000007.13:g.146489714_146489715delinsTA , CM000669.1:g.146489714_146489715delinsTA GRCh37
NC_000007.12:g.146120647_146120648delinsTA NCBI36
NG_007092.2:g.681262_681263delinsTA
NG_007092.3:g.681622_681623delinsTA

Transcript Alleles

HGVS Amino-acid change
ENST00000361727.8:c.208+18241_208+18242delinsTA MANE Select ENSP00000354778.3:n.208+18241_208+18242de...
ENST00000636561.1:n.111+18241_111+18242delinsTA
ENST00000637150.1:n.137+18241_137+18242delinsTA
ENST00000637694.1:n.111+18241_111+18242delinsTA
ENST00000638117.1:n.111+18241_111+18242delinsTA
ENST00000361727.7:c.208+18241_208+18242delinsTA ENSP00000354778.3:n.208+18241_208+18242de...
ENST00000625365.2:c.208+18241_208+18242delinsTA ENSP00000485955.1:n.208+18241_208+18242de...
NM_014141.5:c.208+18241_208+18242delinsTA NP_054860.1:n.208+18241_208+18242delinsTA...
XM_017011950.2:c.208+18241_208+18242delinsTA XP_016867439.1:n.208+18241_208+18242delin...
NM_014141.6:c.208+18241_208+18242delinsTA MANE Select NP_054860.1:n.208+18241_208+18242delinsTA...