Canonical Allele Identifier: CA1750443785

Gene: CNTNAP2

Linked Data

• dbSNP Id: rs2049844635

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.146792571A>T , CM000669.2:g.146792571A>T	GRCh38
NC_000007.13:g.146489663A>T , CM000669.1:g.146489663A>T	GRCh37
NC_000007.12:g.146120596A>T	NCBI36
NG_007092.2:g.681211A>T
NG_007092.3:g.681571A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000361727.8:c.208+18190A>T MANE Select	ENSP00000354778.3:n.208+18190A>T
ENST00000636561.1:n.111+18190A>T
ENST00000637150.1:n.137+18190A>T
ENST00000637694.1:n.111+18190A>T
ENST00000638117.1:n.111+18190A>T
ENST00000361727.7:c.208+18190A>T	ENSP00000354778.3:n.208+18190A>T
ENST00000625365.2:c.208+18190A>T	ENSP00000485955.1:n.208+18190A>T
NM_014141.5:c.208+18190A>T	NP_054860.1:n.208+18190A>T
XM_017011950.2:c.208+18190A>T	XP_016867439.1:n.208+18190A>T
NM_014141.6:c.208+18190A>T MANE Select	NP_054860.1:n.208+18190A>T