Canonical Allele Identifier: CA1750443722

Gene: CNTNAP2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.146792459C= , CM000669.2:g.146792459C=	GRCh38
NC_000007.13:g.146489551C= , CM000669.1:g.146489551C=	GRCh37
NC_000007.12:g.146120484C=	NCBI36
NG_007092.2:g.681099C=
NG_007092.3:g.681459C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000361727.8:c.208+18078C= MANE Select	ENSP00000354778.3:n.208+18078C=
ENST00000636561.1:n.111+18078C=
ENST00000637150.1:n.137+18078C=
ENST00000637694.1:n.111+18078C=
ENST00000638117.1:n.111+18078C=
ENST00000361727.7:c.208+18078C=	ENSP00000354778.3:n.208+18078C=
ENST00000625365.2:c.208+18078C=	ENSP00000485955.1:n.208+18078C=
NM_014141.5:c.208+18078C=	NP_054860.1:n.208+18078C=
XM_017011950.2:c.208+18078C=	XP_016867439.1:n.208+18078C=
NM_014141.6:c.208+18078C= MANE Select	NP_054860.1:n.208+18078C=