Canonical Allele Identifier: CA2576277896

Gene: CNTNAP1 CCR10

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42682797_42682798del , CM000679.2:g.42682797_42682798del	GRCh38
NC_000017.10:g.40834815_40834816del , CM000679.1:g.40834815_40834816del	GRCh37
NC_000017.9:g.38088341_38088342del	NCBI36
NG_042091.1:g.5184_5185del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264638.9:c.-33_-32del (CNTNAP1) MANE Select	ENSP00000264638.3:n.-33_-32del
ENST00000264638.8:c.-33_-32del (CNTNAP1)	ENSP00000264638.3:n.-33_-32del
ENST00000591568.1:c.-643+1020_-643+1021del (CCR10)	ENSP00000467331.1:n.-643+1020_-643+1021del
ENST00000591662.1:c.-33_-32del (CNTNAP1)	ENSP00000466571.1:n.-33_-32del
ENST00000591765.1:c.-1118_-1117del (CCR10)	ENSP00000468135.1:n.-1118_-1117del
NM_003632.2:c.-33_-32del (CNTNAP1)	NP_003623.1:n.-33_-32del
XM_005257748.4:c.-1053_-1052del (CNTNAP1)	XP_005257805.1:n.-1053_-1052del
XM_017025238.1:c.-33_-32del (CNTNAP1)	XP_016880727.1:n.-33_-32del
XM_024451011.1:c.-33_-32del (CNTNAP1)	XP_024306779.1:n.-33_-32del
NM_003632.3:c.-33_-32del (CNTNAP1) MANE Select	NP_003623.1:n.-33_-32del