Canonical Allele Identifier: CA369924513

Gene: CNTNAP2

Linked Data

• MyVariant Identifiers: chr7:g.146829367T>G (hg19) ; chr7:g.147132275T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.147132275T>G , CM000669.2:g.147132275T>G	GRCh38
NC_000007.13:g.146829367T>G , CM000669.1:g.146829367T>G	GRCh37
NC_000007.12:g.146460300T>G	NCBI36
NG_007092.2:g.1020915T>G
NG_007092.3:g.1021275T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361727.8:c.1114T>G MANE Select	ENSP00000354778.3:p.Tyr372Asp
ENST00000636561.1:n.1017T>G
ENST00000636870.1:n.976T>G
ENST00000637150.1:n.1043T>G
ENST00000637694.1:n.1017T>G
ENST00000637825.1:n.597T>G
ENST00000638117.1:n.1017T>G
ENST00000361727.7:c.1114T>G	ENSP00000354778.3:p.Tyr372Asp
NM_014141.5:c.1114T>G	NP_054860.1:p.Tyr372Asp
XM_017011950.2:c.1114T>G	XP_016867439.1:p.Tyr372Asp
NM_014141.6:c.1114T>G MANE Select	NP_054860.1:p.Tyr372Asp