Canonical Allele Identifier: CA2637988612

Gene: CNTNAP1 CCR10

Linked Data

• gnomAD v4: 17-42682635-A-AGT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42682636_42682637insTG , CM000679.2:g.42682636_42682637insTG	GRCh38
NC_000017.10:g.40834654_40834655insTG , CM000679.1:g.40834654_40834655insTG	GRCh37
NC_000017.9:g.38088180_38088181insTG	NCBI36
NG_042091.1:g.5023_5024insTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264638.9:c.-194_-193insTG (CNTNAP1) MANE Select	ENSP00000264638.3:n.-194_-193insTG
ENST00000264638.8:c.-194_-193insTG (CNTNAP1)	ENSP00000264638.3:n.-194_-193insTG
ENST00000591568.1:c.-643+1180_-643+1181insAC (CCR10)	ENSP00000467331.1:n.-643+1180_-643+1181insAC
ENST00000591765.1:c.-958_-957insAC (CCR10)	ENSP00000468135.1:n.-958_-957insAC
NM_003632.2:c.-194_-193insTG (CNTNAP1)	NP_003623.1:n.-194_-193insTG
XM_017025238.1:c.-194_-193insTG (CNTNAP1)	XP_016880727.1:n.-194_-193insTG
XM_024451011.1:c.-194_-193insTG (CNTNAP1)	XP_024306779.1:n.-194_-193insTG
NM_003632.3:c.-194_-193insTG (CNTNAP1) MANE Select	NP_003623.1:n.-194_-193insTG