Canonical Allele Identifier: CA168786661

Gene: CNTNAP2

Linked Data

• dbSNP Id: rs1023744041
• gnomAD v3: 7-147904509-C-T
• gnomAD v4: 7-147904509-C-T
• MyVariant Identifiers: chr7:g.147601601C>T (hg19) ; chr7:g.147904509C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.147904509C>T , CM000669.2:g.147904509C>T	GRCh38
NC_000007.13:g.147601601C>T , CM000669.1:g.147601601C>T	GRCh37
NC_000007.12:g.147232534C>T	NCBI36
NG_007092.2:g.1793149C>T
NG_007092.3:g.1793509C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361727.8:c.2255+788C>T MANE Select	ENSP00000354778.3:n.2255+788C>T
ENST00000636870.1:n.2117+788C>T
ENST00000637825.1:n.1738+788C>T
ENST00000361727.7:c.2255+788C>T	ENSP00000354778.3:n.2255+788C>T
ENST00000455301.2:n.190+788C>T
ENST00000627772.2:n.428+788C>T
NM_014141.5:c.2255+788C>T	NP_054860.1:n.2255+788C>T
XM_006715919.1:c.743+788C>T	XP_006715982.1:n.743+788C>T
NM_014141.6:c.2255+788C>T MANE Select	NP_054860.1:n.2255+788C>T