Canonical Allele Identifier: CA369925016
Gene: CNTNAP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.147132509G>T , CM000669.2:g.147132509G>T GRCh38
NC_000007.13:g.146829601G>T , CM000669.1:g.146829601G>T GRCh37
NC_000007.12:g.146460534G>T NCBI36
NG_007092.2:g.1021149G>T
NG_007092.3:g.1021509G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000361727.8:c.1348G>T MANE Select ENSP00000354778.3:p.Gly450Cys
ENST00000636561.1:n.1251G>T
ENST00000636870.1:n.1210G>T
ENST00000637150.1:n.1277G>T
ENST00000637694.1:n.1251G>T
ENST00000637825.1:n.831G>T
ENST00000638117.1:n.1251G>T
ENST00000361727.7:c.1348G>T ENSP00000354778.3:p.Gly450Cys
NM_014141.5:c.1348G>T NP_054860.1:p.Gly450Cys
XM_017011950.2:c.1348G>T XP_016867439.1:p.Gly450Cys
NM_014141.6:c.1348G>T MANE Select NP_054860.1:p.Gly450Cys