Canonical Allele Identifier: CA369924921

Gene: CNTNAP2

Linked Data

• MyVariant Identifiers: chr7:g.146829559A>C (hg19) ; chr7:g.147132467A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.147132467A>C , CM000669.2:g.147132467A>C	GRCh38
NC_000007.13:g.146829559A>C , CM000669.1:g.146829559A>C	GRCh37
NC_000007.12:g.146460492A>C	NCBI36
NG_007092.2:g.1021107A>C
NG_007092.3:g.1021467A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361727.8:c.1306A>C MANE Select	ENSP00000354778.3:p.Asn436His
ENST00000636561.1:n.1209A>C
ENST00000636870.1:n.1168A>C
ENST00000637150.1:n.1235A>C
ENST00000637694.1:n.1209A>C
ENST00000637825.1:n.789A>C
ENST00000638117.1:n.1209A>C
ENST00000361727.7:c.1306A>C	ENSP00000354778.3:p.Asn436His
NM_014141.5:c.1306A>C	NP_054860.1:p.Asn436His
XM_017011950.2:c.1306A>C	XP_016867439.1:p.Asn436His
NM_014141.6:c.1306A>C MANE Select	NP_054860.1:p.Asn436His