Canonical Allele Identifier: CA369924968

Gene: CNTNAP2

Linked Data

• dbSNP Id: rs1801397036
• MyVariant Identifiers: chr7:g.146829579G>A (hg19) ; chr7:g.147132487G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.147132487G>A , CM000669.2:g.147132487G>A	GRCh38
NC_000007.13:g.146829579G>A , CM000669.1:g.146829579G>A	GRCh37
NC_000007.12:g.146460512G>A	NCBI36
NG_007092.2:g.1021127G>A
NG_007092.3:g.1021487G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361727.8:c.1326G>A MANE Select	ENSP00000354778.3:p.Met442Ile
ENST00000636561.1:n.1229G>A
ENST00000636870.1:n.1188G>A
ENST00000637150.1:n.1255G>A
ENST00000637694.1:n.1229G>A
ENST00000637825.1:n.809G>A
ENST00000638117.1:n.1229G>A
ENST00000361727.7:c.1326G>A	ENSP00000354778.3:p.Met442Ile
NM_014141.5:c.1326G>A	NP_054860.1:p.Met442Ile
XM_017011950.2:c.1326G>A	XP_016867439.1:p.Met442Ile
NM_014141.6:c.1326G>A MANE Select	NP_054860.1:p.Met442Ile