Canonical Allele Identifier: CA2260596055

Gene: CNTNAP1 CCR10

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42682651_42682655delinsAAAAG , CM000679.2:g.42682651_42682655delinsAAAAG	GRCh38
NC_000017.10:g.40834669_40834673delinsAAAAG , CM000679.1:g.40834669_40834673delinsAAAAG	GRCh37
NC_000017.9:g.38088195_38088199delinsAAAAG	NCBI36
NG_042091.1:g.5038_5042delinsAAAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264638.9:c.-179_-175delinsAAAAG (CNTNAP1) MANE Select	ENSP00000264638.3:n.-179_-175delinsAAAAG
ENST00000264638.8:c.-179_-175delinsAAAAG (CNTNAP1)	ENSP00000264638.3:n.-179_-175delinsAAAAG
ENST00000591568.1:c.-643+1161_-643+1165delinsCTTTT (CCR10)	ENSP00000467331.1:n.-643+1161_-643+1165delinsCTTTT
ENST00000591765.1:c.-977_-973delinsCTTTT (CCR10)	ENSP00000468135.1:n.-977_-973delinsCTTTT
NM_003632.2:c.-179_-175delinsAAAAG (CNTNAP1)	NP_003623.1:n.-179_-175delinsAAAAG
XM_005257748.4:c.-1199_-1195delinsAAAAG (CNTNAP1)	XP_005257805.1:n.-1199_-1195delinsAAAAG
XM_017025238.1:c.-179_-175delinsAAAAG (CNTNAP1)	XP_016880727.1:n.-179_-175delinsAAAAG
XM_024451011.1:c.-179_-175delinsAAAAG (CNTNAP1)	XP_024306779.1:n.-179_-175delinsAAAAG
NM_003632.3:c.-179_-175delinsAAAAG (CNTNAP1) MANE Select	NP_003623.1:n.-179_-175delinsAAAAG