Canonical Allele Identifier: CA369924800
Gene: CNTNAP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.147132408C>G , CM000669.2:g.147132408C>G GRCh38
NC_000007.13:g.146829500C>G , CM000669.1:g.146829500C>G GRCh37
NC_000007.12:g.146460433C>G NCBI36
NG_007092.2:g.1021048C>G
NG_007092.3:g.1021408C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000361727.8:c.1247C>G MANE Select ENSP00000354778.3:p.Ala416Gly
ENST00000636561.1:n.1150C>G
ENST00000636870.1:n.1109C>G
ENST00000637150.1:n.1176C>G
ENST00000637694.1:n.1150C>G
ENST00000637825.1:n.730C>G
ENST00000638117.1:n.1150C>G
ENST00000361727.7:c.1247C>G ENSP00000354778.3:p.Ala416Gly
NM_014141.5:c.1247C>G NP_054860.1:p.Ala416Gly
XM_017011950.2:c.1247C>G XP_016867439.1:p.Ala416Gly
NM_014141.6:c.1247C>G MANE Select NP_054860.1:p.Ala416Gly