Canonical Allele Identifier: CA2260596096

Gene: CNTNAP1 CCR10

Linked Data

• dbSNP Id: rs2052950835

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42682726_42682732del , CM000679.2:g.42682726_42682732del	GRCh38
NC_000017.10:g.40834744_40834750del , CM000679.1:g.40834744_40834750del	GRCh37
NC_000017.9:g.38088270_38088276del	NCBI36
NG_042091.1:g.5113_5119del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264638.9:c.-104_-98del (CNTNAP1) MANE Select	ENSP00000264638.3:n.-104_-98del
ENST00000264638.8:c.-104_-98del (CNTNAP1)	ENSP00000264638.3:n.-104_-98del
ENST00000591568.1:c.-643+1086_-643+1092del (CCR10)	ENSP00000467331.1:n.-643+1086_-643+1092del
ENST00000591662.1:c.-104_-98del (CNTNAP1)	ENSP00000466571.1:n.-104_-98del
ENST00000591765.1:c.-1052_-1046del (CCR10)	ENSP00000468135.1:n.-1052_-1046del
NM_003632.2:c.-104_-98del (CNTNAP1)	NP_003623.1:n.-104_-98del
XM_005257748.4:c.-1124_-1118del (CNTNAP1)	XP_005257805.1:n.-1124_-1118del
XM_017025238.1:c.-104_-98del (CNTNAP1)	XP_016880727.1:n.-104_-98del
XM_024451011.1:c.-104_-98del (CNTNAP1)	XP_024306779.1:n.-104_-98del
NM_003632.3:c.-104_-98del (CNTNAP1) MANE Select	NP_003623.1:n.-104_-98del