Canonical Allele Identifier: CA369924417

Gene: CNTNAP2

Linked Data

• ClinVar Variation Id: 1059153
• ClinVar RCV Id: RCV001368380
• dbSNP Id: rs2129284424
• MyVariant Identifiers: chr7:g.146825917C>T (hg19) ; chr7:g.147128825C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.147128825C>T , CM000669.2:g.147128825C>T	GRCh38
NC_000007.13:g.146825917C>T , CM000669.1:g.146825917C>T	GRCh37
NC_000007.12:g.146456850C>T	NCBI36
NG_007092.2:g.1017465C>T
NG_007092.3:g.1017825C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361727.8:c.1072C>T MANE Select	ENSP00000354778.3:p.Pro358Ser
ENST00000636561.1:n.975C>T
ENST00000636870.1:n.934C>T
ENST00000637150.1:n.1001C>T
ENST00000637694.1:n.975C>T
ENST00000637825.1:n.555C>T
ENST00000638117.1:n.975C>T
ENST00000361727.7:c.1072C>T	ENSP00000354778.3:p.Pro358Ser
NM_014141.5:c.1072C>T	NP_054860.1:p.Pro358Ser
XM_017011950.2:c.1072C>T	XP_016867439.1:p.Pro358Ser
NM_014141.6:c.1072C>T MANE Select	NP_054860.1:p.Pro358Ser