Canonical Allele Identifier: CA1750620132

Gene: CNTNAP2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.147128861T= , CM000669.2:g.147128861T=	GRCh38
NC_000007.13:g.146825953T= , CM000669.1:g.146825953T=	GRCh37
NC_000007.12:g.146456886T=	NCBI36
NG_007092.2:g.1017501T=
NG_007092.3:g.1017861T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361727.8:c.1083+25T= MANE Select	ENSP00000354778.3:n.1083+25T=
ENST00000636561.1:n.986+25T=
ENST00000636870.1:n.945+25T=
ENST00000637150.1:n.1012+25T=
ENST00000637694.1:n.986+25T=
ENST00000637825.1:n.566+25T=
ENST00000638117.1:n.986+25T=
ENST00000361727.7:c.1083+25T=	ENSP00000354778.3:n.1083+25T=
NM_014141.5:c.1083+25T=	NP_054860.1:n.1083+25T=
XM_017011950.2:c.1083+25T=	XP_016867439.1:n.1083+25T=
NM_014141.6:c.1083+25T= MANE Select	NP_054860.1:n.1083+25T=