Canonical Allele Identifier: CA1750229691
Gene: CNTNAP2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.146351677C= , CM000669.2:g.146351677C= GRCh38
NC_000007.13:g.146048769C= , CM000669.1:g.146048769C= GRCh37
NC_000007.12:g.145679702C= NCBI36
NG_007092.2:g.240317C=
NG_007092.3:g.240677C=

Transcript Alleles

HGVS Amino-acid change
ENST00000361727.8:c.97+234704C= MANE Select ENSP00000354778.3:n.97+234704C=
ENST00000637150.1:n.26+234704C=
ENST00000361727.7:c.97+234704C= ENSP00000354778.3:n.97+234704C=
ENST00000625365.2:c.97+234704C= ENSP00000485955.1:n.97+234704C=
NM_014141.5:c.97+234704C= NP_054860.1:n.97+234704C=
XM_017011950.2:c.97+234704C= XP_016867439.1:n.97+234704C=
NM_014141.6:c.97+234704C= MANE Select NP_054860.1:n.97+234704C=
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