Canonical Allele Identifier: CA834914598

Gene: CNTNAP2

Linked Data

• dbSNP Id: rs1480342792
• gnomAD v3: 7-147882705-A-G
• gnomAD v4: 7-147882705-A-G
• MyVariant Identifiers: chr7:g.147579797A>G (hg19) ; chr7:g.147882705A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.147882705A>G , CM000669.2:g.147882705A>G	GRCh38
NC_000007.13:g.147579797A>G , CM000669.1:g.147579797A>G	GRCh37
NC_000007.12:g.147210730A>G	NCBI36
NG_007092.2:g.1771345A>G
NG_007092.3:g.1771705A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361727.8:c.2099-20860A>G MANE Select	ENSP00000354778.3:n.2099-20860A>G
ENST00000636870.1:n.1961-20860A>G
ENST00000637825.1:n.1582-20860A>G
ENST00000361727.7:c.2099-20860A>G	ENSP00000354778.3:n.2099-20860A>G
ENST00000455301.2:n.34-20860A>G
ENST00000627772.2:n.272-20860A>G
NM_014141.5:c.2099-20860A>G	NP_054860.1:n.2099-20860A>G
XM_006715919.1:c.587-20860A>G	XP_006715982.1:n.587-20860A>G
NM_014141.6:c.2099-20860A>G MANE Select	NP_054860.1:n.2099-20860A>G