Canonical Allele Identifier: CA1751005487
Gene: CNTNAP2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.147918562C= , CM000669.2:g.147918562C= GRCh38
NC_000007.13:g.147615654C= , CM000669.1:g.147615654C= GRCh37
NC_000007.12:g.147246587C= NCBI36
NG_007092.2:g.1807202C=
NG_007092.3:g.1807562C=

Transcript Alleles

HGVS Amino-acid change
ENST00000361727.8:c.2255+14841C= MANE Select ENSP00000354778.3:n.2255+14841C=
ENST00000636870.1:n.2117+14841C=
ENST00000637825.1:n.1738+14841C=
ENST00000361727.7:c.2255+14841C= ENSP00000354778.3:n.2255+14841C=
ENST00000455301.2:n.190+14841C=
ENST00000627772.2:n.428+14841C=
NM_014141.5:c.2255+14841C= NP_054860.1:n.2255+14841C=
XM_006715919.1:c.743+14841C= XP_006715982.1:n.743+14841C=
NM_014141.6:c.2255+14841C= MANE Select NP_054860.1:n.2255+14841C=
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