Canonical Allele Identifier: CA1750436628

Gene: CNTNAP2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.146778149_146778150delinsCA , CM000669.2:g.146778149_146778150delinsCA	GRCh38
NC_000007.13:g.146475241_146475242delinsCA , CM000669.1:g.146475241_146475242delinsCA	GRCh37
NC_000007.12:g.146106174_146106175delinsCA	NCBI36
NG_007092.2:g.666789_666790delinsCA
NG_007092.3:g.667149_667150delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361727.8:c.208+3768_208+3769delinsCA MANE Select	ENSP00000354778.3:n.208+3768_208+3769delinsCA
ENST00000636277.1:n.75+3768_75+3769delinsCA
ENST00000636561.1:n.111+3768_111+3769delinsCA
ENST00000636600.1:n.58+3768_58+3769delinsCA
ENST00000637150.1:n.137+3768_137+3769delinsCA
ENST00000637694.1:n.111+3768_111+3769delinsCA
ENST00000638117.1:n.111+3768_111+3769delinsCA
ENST00000361727.7:c.208+3768_208+3769delinsCA	ENSP00000354778.3:n.208+3768_208+3769delinsCA
ENST00000625365.2:c.208+3768_208+3769delinsCA	ENSP00000485955.1:n.208+3768_208+3769delinsCA
NM_014141.5:c.208+3768_208+3769delinsCA	NP_054860.1:n.208+3768_208+3769delinsCA
XM_017011950.2:c.208+3768_208+3769delinsCA	XP_016867439.1:n.208+3768_208+3769delinsCA
NM_014141.6:c.208+3768_208+3769delinsCA MANE Select	NP_054860.1:n.208+3768_208+3769delinsCA