Canonical Allele Identifier: CA168784026
Gene: CNTNAP2 HGNC NCBI

Linked Data

dbSNP Id: rs974797026
MyVariant Identifiers: chr7:g.147579888T>C (hg19) chr7:g.147882796T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.147882796T>C , CM000669.2:g.147882796T>C GRCh38
NC_000007.13:g.147579888T>C , CM000669.1:g.147579888T>C GRCh37
NC_000007.12:g.147210821T>C NCBI36
NG_007092.2:g.1771436T>C
NG_007092.3:g.1771796T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000361727.8:c.2099-20769T>C MANE Select ENSP00000354778.3:n.2099-20769T>C
ENST00000636870.1:n.1961-20769T>C
ENST00000637825.1:n.1582-20769T>C
ENST00000361727.7:c.2099-20769T>C ENSP00000354778.3:n.2099-20769T>C
ENST00000455301.2:n.34-20769T>C
ENST00000627772.2:n.272-20769T>C
NM_014141.5:c.2099-20769T>C NP_054860.1:n.2099-20769T>C
XM_006715919.1:c.587-20769T>C XP_006715982.1:n.587-20769T>C
NM_014141.6:c.2099-20769T>C MANE Select NP_054860.1:n.2099-20769T>C
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