Canonical Allele Identifier: CA2260595982

Gene: CCR10 CNTNAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42682527C= , CM000679.2:g.42682527C=	GRCh38
NC_000017.10:g.40834545C= , CM000679.1:g.40834545C=	GRCh37
NC_000017.9:g.38088071C=	NCBI36
NG_042091.1:g.4914C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000591568.1:c.-643+1289G= (CCR10)	ENSP00000467331.1:n.-643+1289G=
ENST00000591765.1:c.-849G= (CCR10)	ENSP00000468135.1:n.-849G=
XM_017025238.1:c.-303C= (CNTNAP1)	XP_016880727.1:n.-303C=
XM_024451011.1:c.-303C= (CNTNAP1)	XP_024306779.1:n.-303C=