Canonical Allele Identifier: CA168786670

Gene: CNTNAP2

Linked Data

• dbSNP Id: rs918169795
• MyVariant Identifiers: chr7:g.147601695G>C (hg19) ; chr7:g.147904603G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.147904603G>C , CM000669.2:g.147904603G>C	GRCh38
NC_000007.13:g.147601695G>C , CM000669.1:g.147601695G>C	GRCh37
NC_000007.12:g.147232628G>C	NCBI36
NG_007092.2:g.1793243G>C
NG_007092.3:g.1793603G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000361727.8:c.2255+882G>C MANE Select	ENSP00000354778.3:n.2255+882G>C
ENST00000636870.1:n.2117+882G>C
ENST00000637825.1:n.1738+882G>C
ENST00000361727.7:c.2255+882G>C	ENSP00000354778.3:n.2255+882G>C
ENST00000455301.2:n.190+882G>C
ENST00000627772.2:n.428+882G>C
NM_014141.5:c.2255+882G>C	NP_054860.1:n.2255+882G>C
XM_006715919.1:c.743+882G>C	XP_006715982.1:n.743+882G>C
NM_014141.6:c.2255+882G>C MANE Select	NP_054860.1:n.2255+882G>C