Canonical Allele Identifier: CA458577933
Gene: CNTNAP2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.146829414C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.147132322C>G , CM000669.2:g.147132322C>G GRCh38
NC_000007.13:g.146829414C>G , CM000669.1:g.146829414C>G GRCh37
NC_000007.12:g.146460347C>G NCBI36
NG_007092.2:g.1020962C>G
NG_007092.3:g.1021322C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000361727.8:c.1161C>G MANE Select ENSP00000354778.3:p.Pro387=
ENST00000636561.1:n.1064C>G
ENST00000636870.1:n.1023C>G
ENST00000637150.1:n.1090C>G
ENST00000637694.1:n.1064C>G
ENST00000637825.1:n.644C>G
ENST00000638117.1:n.1064C>G
ENST00000361727.7:c.1161C>G ENSP00000354778.3:p.Pro387=
NM_014141.5:c.1161C>G NP_054860.1:p.Pro387=
XM_017011950.2:c.1161C>G XP_016867439.1:p.Pro387=
NM_014141.6:c.1161C>G MANE Select NP_054860.1:p.Pro387=
Search 100 bp 5'
Search 100 bp 3'