Canonical Allele Identifier: CA2260595998

Gene: CNTNAP1 CCR10

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42682555G= , CM000679.2:g.42682555G=	GRCh38
NC_000017.10:g.40834573G= , CM000679.1:g.40834573G=	GRCh37
NC_000017.9:g.38088099G=	NCBI36
NG_042091.1:g.4942G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264638.9:c.-275G= (CNTNAP1) MANE Select	ENSP00000264638.3:n.-275G=
ENST00000591568.1:c.-643+1261C= (CCR10)	ENSP00000467331.1:n.-643+1261C=
ENST00000591765.1:c.-877C= (CCR10)	ENSP00000468135.1:n.-877C=
XM_017025238.1:c.-275G= (CNTNAP1)	XP_016880727.1:n.-275G=
XM_024451011.1:c.-275G= (CNTNAP1)	XP_024306779.1:n.-275G=
NM_003632.3:c.-275G= (CNTNAP1) MANE Select	NP_003623.1:n.-275G=