Canonical Allele Identifier: CA1108407721
Gene: CNTNAP2 HGNC NCBI

Linked Data

dbSNP Id: rs1801406286
gnomAD v3: 7-147132882-G-A
gnomAD v4: 7-147132882-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.147132882G>A , CM000669.2:g.147132882G>A GRCh38
NC_000007.13:g.146829974G>A , CM000669.1:g.146829974G>A GRCh37
NC_000007.12:g.146460907G>A NCBI36
NG_007092.2:g.1021522G>A
NG_007092.3:g.1021882G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000361727.8:c.1348+373G>A MANE Select ENSP00000354778.3:n.1348+373G>A
ENST00000636561.1:n.1251+373G>A
ENST00000636870.1:n.1210+373G>A
ENST00000637150.1:n.1277+373G>A
ENST00000637694.1:n.1251+373G>A
ENST00000637825.1:n.831+373G>A
ENST00000638117.1:n.1251+373G>A
ENST00000361727.7:c.1348+373G>A ENSP00000354778.3:n.1348+373G>A
NM_014141.5:c.1348+373G>A NP_054860.1:n.1348+373G>A
XM_017011950.2:c.1348+373G>A XP_016867439.1:n.1348+373G>A
NM_014141.6:c.1348+373G>A MANE Select NP_054860.1:n.1348+373G>A
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