Canonical Allele Identifier: CA369924591
Gene: CNTNAP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.147132311C>G , CM000669.2:g.147132311C>G GRCh38
NC_000007.13:g.146829403C>G , CM000669.1:g.146829403C>G GRCh37
NC_000007.12:g.146460336C>G NCBI36
NG_007092.2:g.1020951C>G
NG_007092.3:g.1021311C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000361727.8:c.1150C>G MANE Select ENSP00000354778.3:p.Leu384Val
ENST00000636561.1:n.1053C>G
ENST00000636870.1:n.1012C>G
ENST00000637150.1:n.1079C>G
ENST00000637694.1:n.1053C>G
ENST00000637825.1:n.633C>G
ENST00000638117.1:n.1053C>G
ENST00000361727.7:c.1150C>G ENSP00000354778.3:p.Leu384Val
NM_014141.5:c.1150C>G NP_054860.1:p.Leu384Val
XM_017011950.2:c.1150C>G XP_016867439.1:p.Leu384Val
NM_014141.6:c.1150C>G MANE Select NP_054860.1:p.Leu384Val