Canonical Allele Identifier: CA1750623602

Gene: CNTNAP2

Linked Data

• dbSNP Id: rs1801387467

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.147132165A>C , CM000669.2:g.147132165A>C	GRCh38
NC_000007.13:g.146829257A>C , CM000669.1:g.146829257A>C	GRCh37
NC_000007.12:g.146460190A>C	NCBI36
NG_007092.2:g.1020805A>C
NG_007092.3:g.1021165A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361727.8:c.1084-80A>C MANE Select	ENSP00000354778.3:n.1084-80A>C
ENST00000636561.1:n.987-80A>C
ENST00000636870.1:n.946-80A>C
ENST00000637150.1:n.1013-80A>C
ENST00000637694.1:n.987-80A>C
ENST00000637825.1:n.567-80A>C
ENST00000638117.1:n.987-80A>C
ENST00000361727.7:c.1084-80A>C	ENSP00000354778.3:n.1084-80A>C
NM_014141.5:c.1084-80A>C	NP_054860.1:n.1084-80A>C
XM_017011950.2:c.1084-80A>C	XP_016867439.1:n.1084-80A>C
NM_014141.6:c.1084-80A>C MANE Select	NP_054860.1:n.1084-80A>C