Canonical Allele Identifier: CA1750654891
Gene: CNTNAP2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.147200377C= , CM000669.2:g.147200377C= GRCh38
NC_000007.13:g.146897469C= , CM000669.1:g.146897469C= GRCh37
NC_000007.12:g.146528402C= NCBI36
NG_007092.2:g.1089017C=
NG_007092.3:g.1089377C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361727.8:c.1348+67868C= MANE Select ENSP00000354778.3:n.1348+67868C=
ENST00000636870.1:n.1210+67868C=
ENST00000637694.1:n.1251+67868C=
ENST00000637825.1:n.831+67868C=
ENST00000638117.1:n.1251+67868C=
ENST00000361727.7:c.1348+67868C= ENSP00000354778.3:n.1348+67868C=
NM_014141.5:c.1348+67868C= NP_054860.1:n.1348+67868C=
XM_017011950.2:c.1348+67868C= XP_016867439.1:n.1348+67868C=
NM_014141.6:c.1348+67868C= MANE Select NP_054860.1:n.1348+67868C=
Search 100 bp 5'
Search 100 bp 3'