Canonical Allele Identifier: CA458577761

Gene: CNTNAP2

Linked Data

• MyVariant Identifiers: chr7:g.146829339A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.147132247A>G , CM000669.2:g.147132247A>G	GRCh38
NC_000007.13:g.146829339A>G , CM000669.1:g.146829339A>G	GRCh37
NC_000007.12:g.146460272A>G	NCBI36
NG_007092.2:g.1020887A>G
NG_007092.3:g.1021247A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000361727.8:c.1086A>G MANE Select	ENSP00000354778.3:p.Gly362=
ENST00000636561.1:n.989A>G
ENST00000636870.1:n.948A>G
ENST00000637150.1:n.1015A>G
ENST00000637694.1:n.989A>G
ENST00000637825.1:n.569A>G
ENST00000638117.1:n.989A>G
ENST00000361727.7:c.1086A>G	ENSP00000354778.3:p.Gly362=
NM_014141.5:c.1086A>G	NP_054860.1:p.Gly362=
XM_017011950.2:c.1086A>G	XP_016867439.1:p.Gly362=
NM_014141.6:c.1086A>G MANE Select	NP_054860.1:p.Gly362=