Canonical Allele Identifier: CA2260596026

Gene: CNTNAP1 CCR10

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42682612A= , CM000679.2:g.42682612A=	GRCh38
NC_000017.10:g.40834630A= , CM000679.1:g.40834630A=	GRCh37
NC_000017.9:g.38088156A=	NCBI36
NG_042091.1:g.4999A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264638.9:c.-218A= (CNTNAP1) MANE Select	ENSP00000264638.3:n.-218A=
ENST00000591568.1:c.-643+1204T= (CCR10)	ENSP00000467331.1:n.-643+1204T=
ENST00000591765.1:c.-934T= (CCR10)	ENSP00000468135.1:n.-934T=
XM_017025238.1:c.-218A= (CNTNAP1)	XP_016880727.1:n.-218A=
XM_024451011.1:c.-218A= (CNTNAP1)	XP_024306779.1:n.-218A=
NM_003632.3:c.-218A= (CNTNAP1) MANE Select	NP_003623.1:n.-218A=