Canonical Allele Identifier: CA2637988693

Gene: CNTNAP1 CCR10

Linked Data

• gnomAD v4: 17-42682652-A-AC

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42682652_42682653insC , CM000679.2:g.42682652_42682653insC	GRCh38
NC_000017.10:g.40834670_40834671insC , CM000679.1:g.40834670_40834671insC	GRCh37
NC_000017.9:g.38088196_38088197insC	NCBI36
NG_042091.1:g.5039_5040insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264638.9:c.-178_-177insC (CNTNAP1) MANE Select	ENSP00000264638.3:n.-178_-177insC
ENST00000264638.8:c.-178_-177insC (CNTNAP1)	ENSP00000264638.3:n.-178_-177insC
ENST00000591568.1:c.-643+1163_-643+1164insG (CCR10)	ENSP00000467331.1:n.-643+1163_-643+1164insG
ENST00000591765.1:c.-975_-974insG (CCR10)	ENSP00000468135.1:n.-975_-974insG
NM_003632.2:c.-178_-177insC (CNTNAP1)	NP_003623.1:n.-178_-177insC
XM_005257748.4:c.-1198_-1197insC (CNTNAP1)	XP_005257805.1:n.-1198_-1197insC
XM_017025238.1:c.-178_-177insC (CNTNAP1)	XP_016880727.1:n.-178_-177insC
XM_024451011.1:c.-178_-177insC (CNTNAP1)	XP_024306779.1:n.-178_-177insC
NM_003632.3:c.-178_-177insC (CNTNAP1) MANE Select	NP_003623.1:n.-178_-177insC