Canonical Allele Identifier: CA834929621

Gene: CNTNAP2

Linked Data

• dbSNP Id: rs1405971474
• gnomAD v3: 7-147918587-T-C
• gnomAD v4: 7-147918587-T-C
• MyVariant Identifiers: chr7:g.147615679T>C (hg19) ; chr7:g.147918587T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.147918587T>C , CM000669.2:g.147918587T>C	GRCh38
NC_000007.13:g.147615679T>C , CM000669.1:g.147615679T>C	GRCh37
NC_000007.12:g.147246612T>C	NCBI36
NG_007092.2:g.1807227T>C
NG_007092.3:g.1807587T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000361727.8:c.2255+14866T>C MANE Select	ENSP00000354778.3:n.2255+14866T>C
ENST00000636870.1:n.2117+14866T>C
ENST00000637825.1:n.1738+14866T>C
ENST00000361727.7:c.2255+14866T>C	ENSP00000354778.3:n.2255+14866T>C
ENST00000455301.2:n.190+14866T>C
ENST00000627772.2:n.428+14866T>C
NM_014141.5:c.2255+14866T>C	NP_054860.1:n.2255+14866T>C
XM_006715919.1:c.743+14866T>C	XP_006715982.1:n.743+14866T>C
NM_014141.6:c.2255+14866T>C MANE Select	NP_054860.1:n.2255+14866T>C