Canonical Allele Identifier: CA2260596067

Gene: CNTNAP1 CCR10

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42682677_42682678delinsTG , CM000679.2:g.42682677_42682678delinsTG	GRCh38
NC_000017.10:g.40834695_40834696delinsTG , CM000679.1:g.40834695_40834696delinsTG	GRCh37
NC_000017.9:g.38088221_38088222delinsTG	NCBI36
NG_042091.1:g.5064_5065delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264638.9:c.-153_-152delinsTG (CNTNAP1) MANE Select	ENSP00000264638.3:n.-153_-152delinsTG
ENST00000264638.8:c.-153_-152delinsTG (CNTNAP1)	ENSP00000264638.3:n.-153_-152delinsTG
ENST00000591568.1:c.-643+1138_-643+1139delinsCA (CCR10)	ENSP00000467331.1:n.-643+1138_-643+1139delinsCA
ENST00000591765.1:c.-1000_-999delinsCA (CCR10)	ENSP00000468135.1:n.-1000_-999delinsCA
NM_003632.2:c.-153_-152delinsTG (CNTNAP1)	NP_003623.1:n.-153_-152delinsTG
XM_005257748.4:c.-1173_-1172delinsTG (CNTNAP1)	XP_005257805.1:n.-1173_-1172delinsTG
XM_017025238.1:c.-153_-152delinsTG (CNTNAP1)	XP_016880727.1:n.-153_-152delinsTG
XM_024451011.1:c.-153_-152delinsTG (CNTNAP1)	XP_024306779.1:n.-153_-152delinsTG
NM_003632.3:c.-153_-152delinsTG (CNTNAP1) MANE Select	NP_003623.1:n.-153_-152delinsTG