Canonical Allele Identifier: CA168690936

Gene: CNTNAP2

Linked Data

• dbSNP Id: rs567718986
• gnomAD v2: 7-146829820-G-C
• gnomAD v3: 7-147132728-G-C
• gnomAD v4: 7-147132728-G-C
• MyVariant Identifiers: chr7:g.146829820G>C (hg19) ; chr7:g.147132728G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.147132728G>C , CM000669.2:g.147132728G>C	GRCh38
NC_000007.13:g.146829820G>C , CM000669.1:g.146829820G>C	GRCh37
NC_000007.12:g.146460753G>C	NCBI36
NG_007092.2:g.1021368G>C
NG_007092.3:g.1021728G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361727.8:c.1348+219G>C MANE Select	ENSP00000354778.3:n.1348+219G>C
ENST00000636561.1:n.1251+219G>C
ENST00000636870.1:n.1210+219G>C
ENST00000637150.1:n.1277+219G>C
ENST00000637694.1:n.1251+219G>C
ENST00000637825.1:n.831+219G>C
ENST00000638117.1:n.1251+219G>C
ENST00000361727.7:c.1348+219G>C	ENSP00000354778.3:n.1348+219G>C
NM_014141.5:c.1348+219G>C	NP_054860.1:n.1348+219G>C
XM_017011950.2:c.1348+219G>C	XP_016867439.1:n.1348+219G>C
NM_014141.6:c.1348+219G>C MANE Select	NP_054860.1:n.1348+219G>C