Canonical Allele Identifier: CA290792899

Gene: CNTNAP1

Linked Data

• dbSNP Id: rs942894105
• gnomAD v3: 17-42687504-G-A
• gnomAD v4: 17-42687504-G-A
• MyVariant Identifiers: chr17:g.40839522G>A (hg19) ; chr17:g.42687504G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42687504G>A , CM000679.2:g.42687504G>A	GRCh38
NC_000017.10:g.40839522G>A , CM000679.1:g.40839522G>A	GRCh37
NC_000017.9:g.38093048G>A	NCBI36
NG_042091.1:g.9891G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264638.9:c.1045-216G>A MANE Select	ENSP00000264638.3:n.1045-216G>A
ENST00000264638.8:c.1045-216G>A	ENSP00000264638.3:n.1045-216G>A
ENST00000586801.1:n.244G>A
ENST00000591662.1:c.1045-216G>A	ENSP00000466571.1:n.1045-216G>A
NM_003632.2:c.1045-216G>A	NP_003623.1:n.1045-216G>A
XM_005257748.3:c.817-216G>A	XP_005257805.1:n.817-216G>A
XM_005257748.4:c.817-216G>A	XP_005257805.1:n.817-216G>A
XM_017025238.1:c.1045-216G>A	XP_016880727.1:n.1045-216G>A
XM_024451011.1:c.1045-216G>A	XP_024306779.1:n.1045-216G>A
NM_003632.3:c.1045-216G>A MANE Select	NP_003623.1:n.1045-216G>A