Canonical Allele Identifier: CA578629192

Gene: CNTNAP2

Linked Data

• dbSNP Id: rs1214902277
• gnomAD v2: 7-146829628-T-C
• gnomAD v4: 7-147132536-T-C
• MyVariant Identifiers: chr7:g.146829628T>C (hg19) ; chr7:g.147132536T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.147132536T>C , CM000669.2:g.147132536T>C	GRCh38
NC_000007.13:g.146829628T>C , CM000669.1:g.146829628T>C	GRCh37
NC_000007.12:g.146460561T>C	NCBI36
NG_007092.2:g.1021176T>C
NG_007092.3:g.1021536T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000361727.8:c.1348+27T>C MANE Select	ENSP00000354778.3:n.1348+27T>C
ENST00000636561.1:n.1251+27T>C
ENST00000636870.1:n.1210+27T>C
ENST00000637150.1:n.1277+27T>C
ENST00000637694.1:n.1251+27T>C
ENST00000637825.1:n.831+27T>C
ENST00000638117.1:n.1251+27T>C
ENST00000361727.7:c.1348+27T>C	ENSP00000354778.3:n.1348+27T>C
NM_014141.5:c.1348+27T>C	NP_054860.1:n.1348+27T>C
XM_017011950.2:c.1348+27T>C	XP_016867439.1:n.1348+27T>C
NM_014141.6:c.1348+27T>C MANE Select	NP_054860.1:n.1348+27T>C