Canonical Allele Identifier: CA1750443746
Gene: CNTNAP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.146792494_146792495delinsCA , CM000669.2:g.146792494_146792495delinsCA GRCh38
NC_000007.13:g.146489586_146489587delinsCA , CM000669.1:g.146489586_146489587delinsCA GRCh37
NC_000007.12:g.146120519_146120520delinsCA NCBI36
NG_007092.2:g.681134_681135delinsCA
NG_007092.3:g.681494_681495delinsCA

Transcript Alleles

HGVS Amino-acid change
ENST00000361727.8:c.208+18113_208+18114delinsCA MANE Select ENSP00000354778.3:n.208+18113_208+18114de...
ENST00000636561.1:n.111+18113_111+18114delinsCA
ENST00000637150.1:n.137+18113_137+18114delinsCA
ENST00000637694.1:n.111+18113_111+18114delinsCA
ENST00000638117.1:n.111+18113_111+18114delinsCA
ENST00000361727.7:c.208+18113_208+18114delinsCA ENSP00000354778.3:n.208+18113_208+18114de...
ENST00000625365.2:c.208+18113_208+18114delinsCA ENSP00000485955.1:n.208+18113_208+18114de...
NM_014141.5:c.208+18113_208+18114delinsCA NP_054860.1:n.208+18113_208+18114delinsCA...
XM_017011950.2:c.208+18113_208+18114delinsCA XP_016867439.1:n.208+18113_208+18114delin...
NM_014141.6:c.208+18113_208+18114delinsCA MANE Select NP_054860.1:n.208+18113_208+18114delinsCA...