Canonical Allele Identifier: CA2637974344

Gene: CNTNAP1

Linked Data

• gnomAD v4: 17-42687602-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42687602C>T , CM000679.2:g.42687602C>T	GRCh38
NC_000017.10:g.40839620C>T , CM000679.1:g.40839620C>T	GRCh37
NC_000017.9:g.38093146C>T	NCBI36
NG_042091.1:g.9989C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264638.9:c.1045-118C>T MANE Select	ENSP00000264638.3:n.1045-118C>T
ENST00000264638.8:c.1045-118C>T	ENSP00000264638.3:n.1045-118C>T
ENST00000586801.1:n.342C>T
ENST00000591662.1:c.1045-118C>T	ENSP00000466571.1:n.1045-118C>T
NM_003632.2:c.1045-118C>T	NP_003623.1:n.1045-118C>T
XM_005257748.3:c.817-118C>T	XP_005257805.1:n.817-118C>T
XM_005257748.4:c.817-118C>T	XP_005257805.1:n.817-118C>T
XM_017025238.1:c.1045-118C>T	XP_016880727.1:n.1045-118C>T
XM_024451011.1:c.1045-118C>T	XP_024306779.1:n.1045-118C>T
NM_003632.3:c.1045-118C>T MANE Select	NP_003623.1:n.1045-118C>T