Canonical Allele Identifier: CA1750654797
Gene: CNTNAP2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.147200194G= , CM000669.2:g.147200194G= GRCh38
NC_000007.13:g.146897286G= , CM000669.1:g.146897286G= GRCh37
NC_000007.12:g.146528219G= NCBI36
NG_007092.2:g.1088834G=
NG_007092.3:g.1089194G=

Transcript Alleles

HGVS Amino-acid change
ENST00000361727.8:c.1348+67685G= MANE Select ENSP00000354778.3:n.1348+67685G=
ENST00000636870.1:n.1210+67685G=
ENST00000637694.1:n.1251+67685G=
ENST00000637825.1:n.831+67685G=
ENST00000638117.1:n.1251+67685G=
ENST00000361727.7:c.1348+67685G= ENSP00000354778.3:n.1348+67685G=
NM_014141.5:c.1348+67685G= NP_054860.1:n.1348+67685G=
XM_017011950.2:c.1348+67685G= XP_016867439.1:n.1348+67685G=
NM_014141.6:c.1348+67685G= MANE Select NP_054860.1:n.1348+67685G=
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