Canonical Allele Identifier: CA369925802

Gene: CNTNAP2

Linked Data

• MyVariant Identifiers: chr7:g.147183032T>A (hg19) ; chr7:g.147485940T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.147485940T>A , CM000669.2:g.147485940T>A	GRCh38
NC_000007.13:g.147183032T>A , CM000669.1:g.147183032T>A	GRCh37
NC_000007.12:g.146813965T>A	NCBI36
NG_007092.2:g.1374580T>A
NG_007092.3:g.1374940T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000361727.8:c.1676T>A MANE Select	ENSP00000354778.3:p.Val559Glu
ENST00000636870.1:n.1538T>A
ENST00000637694.1:n.1579T>A
ENST00000637825.1:n.1159T>A
ENST00000638117.1:n.1579T>A
ENST00000361727.7:c.1676T>A	ENSP00000354778.3:p.Val559Glu
NM_014141.5:c.1676T>A	NP_054860.1:p.Val559Glu
XM_006715919.1:c.164T>A	XP_006715982.1:p.Val55Glu
XM_017011950.2:c.1676T>A	XP_016867439.1:p.Val559Glu
NM_014141.6:c.1676T>A MANE Select	NP_054860.1:p.Val559Glu