Canonical Allele Identifier: CA2260596021

Gene: CNTNAP1 CCR10

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42682607G= , CM000679.2:g.42682607G=	GRCh38
NC_000017.10:g.40834625G= , CM000679.1:g.40834625G=	GRCh37
NC_000017.9:g.38088151G=	NCBI36
NG_042091.1:g.4994G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264638.9:c.-223G= (CNTNAP1) MANE Select	ENSP00000264638.3:n.-223G=
ENST00000591568.1:c.-643+1209C= (CCR10)	ENSP00000467331.1:n.-643+1209C=
ENST00000591765.1:c.-929C= (CCR10)	ENSP00000468135.1:n.-929C=
XM_017025238.1:c.-223G= (CNTNAP1)	XP_016880727.1:n.-223G=
XM_024451011.1:c.-223G= (CNTNAP1)	XP_024306779.1:n.-223G=
NM_003632.3:c.-223G= (CNTNAP1) MANE Select	NP_003623.1:n.-223G=