Canonical Allele Identifier: CA1751005486
Gene: CNTNAP2 HGNC NCBI

Linked Data

dbSNP Id: rs1800203172
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.147918558A>G , CM000669.2:g.147918558A>G GRCh38
NC_000007.13:g.147615650A>G , CM000669.1:g.147615650A>G GRCh37
NC_000007.12:g.147246583A>G NCBI36
NG_007092.2:g.1807198A>G
NG_007092.3:g.1807558A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000361727.8:c.2255+14837A>G MANE Select ENSP00000354778.3:n.2255+14837A>G
ENST00000636870.1:n.2117+14837A>G
ENST00000637825.1:n.1738+14837A>G
ENST00000361727.7:c.2255+14837A>G ENSP00000354778.3:n.2255+14837A>G
ENST00000455301.2:n.190+14837A>G
ENST00000627772.2:n.428+14837A>G
NM_014141.5:c.2255+14837A>G NP_054860.1:n.2255+14837A>G
XM_006715919.1:c.743+14837A>G XP_006715982.1:n.743+14837A>G
NM_014141.6:c.2255+14837A>G MANE Select NP_054860.1:n.2255+14837A>G
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