Canonical Allele Identifier: CA2260596128

Gene: CNTNAP1 CCR10

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42682798_42682799delinsAG , CM000679.2:g.42682798_42682799delinsAG	GRCh38
NC_000017.10:g.40834816_40834817delinsAG , CM000679.1:g.40834816_40834817delinsAG	GRCh37
NC_000017.9:g.38088342_38088343delinsAG	NCBI36
NG_042091.1:g.5185_5186delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264638.9:c.-32_-31delinsAG (CNTNAP1) MANE Select	ENSP00000264638.3:n.-32_-31delinsAG
ENST00000264638.8:c.-32_-31delinsAG (CNTNAP1)	ENSP00000264638.3:n.-32_-31delinsAG
ENST00000591568.1:c.-643+1017_-643+1018delinsCT (CCR10)	ENSP00000467331.1:n.-643+1017_-643+1018delinsCT
ENST00000591662.1:c.-32_-31delinsAG (CNTNAP1)	ENSP00000466571.1:n.-32_-31delinsAG
ENST00000591765.1:c.-1121_-1120delinsCT (CCR10)	ENSP00000468135.1:n.-1121_-1120delinsCT
NM_003632.2:c.-32_-31delinsAG (CNTNAP1)	NP_003623.1:n.-32_-31delinsAG
XM_005257748.4:c.-1052_-1051delinsAG (CNTNAP1)	XP_005257805.1:n.-1052_-1051delinsAG
XM_017025238.1:c.-32_-31delinsAG (CNTNAP1)	XP_016880727.1:n.-32_-31delinsAG
XM_024451011.1:c.-32_-31delinsAG (CNTNAP1)	XP_024306779.1:n.-32_-31delinsAG
NM_003632.3:c.-32_-31delinsAG (CNTNAP1) MANE Select	NP_003623.1:n.-32_-31delinsAG