Canonical Allele Identifier: CA652039476
Gene: CNTNAP2 HGNC NCBI

Linked Data

COSMIC: COSN23152815
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.147904392T>A , CM000669.2:g.147904392T>A GRCh38
NC_000007.13:g.147601484T>A , CM000669.1:g.147601484T>A GRCh37
NC_000007.12:g.147232417T>A NCBI36
NG_007092.2:g.1793032T>A
NG_007092.3:g.1793392T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000361727.8:c.2255+671T>A MANE Select ENSP00000354778.3:n.2255+671T>A
ENST00000636870.1:n.2117+671T>A
ENST00000637825.1:n.1738+671T>A
ENST00000361727.7:c.2255+671T>A ENSP00000354778.3:n.2255+671T>A
ENST00000455301.2:n.190+671T>A
ENST00000627772.2:n.428+671T>A
NM_014141.5:c.2255+671T>A NP_054860.1:n.2255+671T>A
XM_006715919.1:c.743+671T>A XP_006715982.1:n.743+671T>A
NM_014141.6:c.2255+671T>A MANE Select NP_054860.1:n.2255+671T>A
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