Canonical Allele Identifier: CA458577970

Gene: CNTNAP2

Linked Data

• MyVariant Identifiers: chr7:g.146829546G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.147132454G>T , CM000669.2:g.147132454G>T	GRCh38
NC_000007.13:g.146829546G>T , CM000669.1:g.146829546G>T	GRCh37
NC_000007.12:g.146460479G>T	NCBI36
NG_007092.2:g.1021094G>T
NG_007092.3:g.1021454G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361727.8:c.1293G>T MANE Select	ENSP00000354778.3:p.Val431=
ENST00000636561.1:n.1196G>T
ENST00000636870.1:n.1155G>T
ENST00000637150.1:n.1222G>T
ENST00000637694.1:n.1196G>T
ENST00000637825.1:n.776G>T
ENST00000638117.1:n.1196G>T
ENST00000361727.7:c.1293G>T	ENSP00000354778.3:p.Val431=
NM_014141.5:c.1293G>T	NP_054860.1:p.Val431=
XM_017011950.2:c.1293G>T	XP_016867439.1:p.Val431=
NM_014141.6:c.1293G>T MANE Select	NP_054860.1:p.Val431=