Canonical Allele Identifier: CA458577762
Gene: CNTNAP2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.146829339A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.147132247A>C , CM000669.2:g.147132247A>C GRCh38
NC_000007.13:g.146829339A>C , CM000669.1:g.146829339A>C GRCh37
NC_000007.12:g.146460272A>C NCBI36
NG_007092.2:g.1020887A>C
NG_007092.3:g.1021247A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000361727.8:c.1086A>C MANE Select ENSP00000354778.3:p.Gly362=
ENST00000636561.1:n.989A>C
ENST00000636870.1:n.948A>C
ENST00000637150.1:n.1015A>C
ENST00000637694.1:n.989A>C
ENST00000637825.1:n.569A>C
ENST00000638117.1:n.989A>C
ENST00000361727.7:c.1086A>C ENSP00000354778.3:p.Gly362=
NM_014141.5:c.1086A>C NP_054860.1:p.Gly362=
XM_017011950.2:c.1086A>C XP_016867439.1:p.Gly362=
NM_014141.6:c.1086A>C MANE Select NP_054860.1:p.Gly362=
Search 100 bp 5'
Search 100 bp 3'