Canonical Allele Identifier: CA168735771

Gene: CNTNAP2

Linked Data

• dbSNP Id: rs569533920
• gnomAD v3: 7-147492513-T-G
• gnomAD v4: 7-147492513-T-G
• MyVariant Identifiers: chr7:g.147189605T>G (hg19) ; chr7:g.147492513T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.147492513T>G , CM000669.2:g.147492513T>G	GRCh38
NC_000007.13:g.147189605T>G , CM000669.1:g.147189605T>G	GRCh37
NC_000007.12:g.146820538T>G	NCBI36
NG_007092.2:g.1381153T>G
NG_007092.3:g.1381513T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361727.8:c.1777+6472T>G MANE Select	ENSP00000354778.3:n.1777+6472T>G
ENST00000636870.1:n.1639+6472T>G
ENST00000637694.1:n.1681-4108T>G
ENST00000637825.1:n.1260+6472T>G
ENST00000638117.1:n.1680+6472T>G
ENST00000361727.7:c.1777+6472T>G	ENSP00000354778.3:n.1777+6472T>G
NM_014141.5:c.1777+6472T>G	NP_054860.1:n.1777+6472T>G
XM_006715919.1:c.265+6472T>G	XP_006715982.1:n.265+6472T>G
XM_017011950.2:c.1777+6472T>G	XP_016867439.1:n.1777+6472T>G
NM_014141.6:c.1777+6472T>G MANE Select	NP_054860.1:n.1777+6472T>G