Canonical Allele Identifier: CA2260596058

Gene: CNTNAP1 CCR10

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42682653_42682655delinsAAG , CM000679.2:g.42682653_42682655delinsAAG	GRCh38
NC_000017.10:g.40834671_40834673delinsAAG , CM000679.1:g.40834671_40834673delinsAAG	GRCh37
NC_000017.9:g.38088197_38088199delinsAAG	NCBI36
NG_042091.1:g.5040_5042delinsAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264638.9:c.-177_-175delinsAAG (CNTNAP1) MANE Select	ENSP00000264638.3:n.-177_-175delinsAAG
ENST00000264638.8:c.-177_-175delinsAAG (CNTNAP1)	ENSP00000264638.3:n.-177_-175delinsAAG
ENST00000591568.1:c.-643+1161_-643+1163delinsCTT (CCR10)	ENSP00000467331.1:n.-643+1161_-643+1163delinsCTT
ENST00000591765.1:c.-977_-975delinsCTT (CCR10)	ENSP00000468135.1:n.-977_-975delinsCTT
NM_003632.2:c.-177_-175delinsAAG (CNTNAP1)	NP_003623.1:n.-177_-175delinsAAG
XM_005257748.4:c.-1197_-1195delinsAAG (CNTNAP1)	XP_005257805.1:n.-1197_-1195delinsAAG
XM_017025238.1:c.-177_-175delinsAAG (CNTNAP1)	XP_016880727.1:n.-177_-175delinsAAG
XM_024451011.1:c.-177_-175delinsAAG (CNTNAP1)	XP_024306779.1:n.-177_-175delinsAAG
NM_003632.3:c.-177_-175delinsAAG (CNTNAP1) MANE Select	NP_003623.1:n.-177_-175delinsAAG