Canonical Allele Identifier: CA834867155
Gene: CNTNAP2 HGNC NCBI

Linked Data

dbSNP Id: rs1397125999
MyVariant Identifiers: chr7:g.146897326G>C (hg19) chr7:g.147200234G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.147200234G>C , CM000669.2:g.147200234G>C GRCh38
NC_000007.13:g.146897326G>C , CM000669.1:g.146897326G>C GRCh37
NC_000007.12:g.146528259G>C NCBI36
NG_007092.2:g.1088874G>C
NG_007092.3:g.1089234G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000361727.8:c.1348+67725G>C MANE Select ENSP00000354778.3:n.1348+67725G>C
ENST00000636870.1:n.1210+67725G>C
ENST00000637694.1:n.1251+67725G>C
ENST00000637825.1:n.831+67725G>C
ENST00000638117.1:n.1251+67725G>C
ENST00000361727.7:c.1348+67725G>C ENSP00000354778.3:n.1348+67725G>C
NM_014141.5:c.1348+67725G>C NP_054860.1:n.1348+67725G>C
XM_017011950.2:c.1348+67725G>C XP_016867439.1:n.1348+67725G>C
NM_014141.6:c.1348+67725G>C MANE Select NP_054860.1:n.1348+67725G>C
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