Canonical Allele Identifier: CA16318150
Gene: CNTNAP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.146262151T>G , CM000669.2:g.146262151T>G GRCh38
NC_000007.13:g.145959243T>G , CM000669.1:g.145959243T>G GRCh37
NC_000007.12:g.145590176T>G NCBI36
NG_007092.2:g.150791T>G
NG_007092.3:g.151151T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000361727.8:c.97+145178T>G MANE Select ENSP00000354778.3:n.97+145178T>G
ENST00000637150.1:n.26+145178T>G
ENST00000361727.7:c.97+145178T>G ENSP00000354778.3:n.97+145178T>G
ENST00000625365.2:c.97+145178T>G ENSP00000485955.1:n.97+145178T>G
NM_014141.5:c.97+145178T>G NP_054860.1:n.97+145178T>G
XM_017011950.2:c.97+145178T>G XP_016867439.1:n.97+145178T>G
NM_014141.6:c.97+145178T>G MANE Select NP_054860.1:n.97+145178T>G