Canonical Allele Identifier: CA168788383
Gene: CNTNAP2 HGNC NCBI

Linked Data

dbSNP Id: rs918437774
MyVariant Identifiers: chr7:g.147615662G>A (hg19) chr7:g.147918570G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.147918570G>A , CM000669.2:g.147918570G>A GRCh38
NC_000007.13:g.147615662G>A , CM000669.1:g.147615662G>A GRCh37
NC_000007.12:g.147246595G>A NCBI36
NG_007092.2:g.1807210G>A
NG_007092.3:g.1807570G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000361727.8:c.2255+14849G>A MANE Select ENSP00000354778.3:n.2255+14849G>A
ENST00000636870.1:n.2117+14849G>A
ENST00000637825.1:n.1738+14849G>A
ENST00000361727.7:c.2255+14849G>A ENSP00000354778.3:n.2255+14849G>A
ENST00000455301.2:n.190+14849G>A
ENST00000627772.2:n.428+14849G>A
NM_014141.5:c.2255+14849G>A NP_054860.1:n.2255+14849G>A
XM_006715919.1:c.743+14849G>A XP_006715982.1:n.743+14849G>A
NM_014141.6:c.2255+14849G>A MANE Select NP_054860.1:n.2255+14849G>A
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