Canonical Allele Identifier: CA1750443708

Gene: CNTNAP2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.146792429G= , CM000669.2:g.146792429G=	GRCh38
NC_000007.13:g.146489521G= , CM000669.1:g.146489521G=	GRCh37
NC_000007.12:g.146120454G=	NCBI36
NG_007092.2:g.681069G=
NG_007092.3:g.681429G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000361727.8:c.208+18048G= MANE Select	ENSP00000354778.3:n.208+18048G=
ENST00000636561.1:n.111+18048G=
ENST00000637150.1:n.137+18048G=
ENST00000637694.1:n.111+18048G=
ENST00000638117.1:n.111+18048G=
ENST00000361727.7:c.208+18048G=	ENSP00000354778.3:n.208+18048G=
ENST00000625365.2:c.208+18048G=	ENSP00000485955.1:n.208+18048G=
NM_014141.5:c.208+18048G=	NP_054860.1:n.208+18048G=
XM_017011950.2:c.208+18048G=	XP_016867439.1:n.208+18048G=
NM_014141.6:c.208+18048G= MANE Select	NP_054860.1:n.208+18048G=