Canonical Allele Identifier: CA2260596158

Gene: CNTNAP1 CCR10

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42682848T= , CM000679.2:g.42682848T=	GRCh38
NC_000017.10:g.40834866T= , CM000679.1:g.40834866T=	GRCh37
NC_000017.9:g.38088392T=	NCBI36
NG_042091.1:g.5235T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264638.9:c.19T= (CNTNAP1) MANE Select	ENSP00000264638.3:p.Phe7=
ENST00000264638.8:c.19T= (CNTNAP1)	ENSP00000264638.3:p.Phe7=
ENST00000591568.1:c.-643+968A= (CCR10)	ENSP00000467331.1:n.-643+968A=
ENST00000591662.1:c.19T= (CNTNAP1)	ENSP00000466571.1:p.Phe7=
ENST00000591765.1:c.-1170A= (CCR10)	ENSP00000468135.1:n.-1170A=
NM_003632.2:c.19T= (CNTNAP1)	NP_003623.1:p.Phe7=
XM_005257748.4:c.-1002T= (CNTNAP1)	XP_005257805.1:n.-1002T=
XM_017025238.1:c.19T= (CNTNAP1)	XP_016880727.1:p.Phe7=
XM_024451011.1:c.19T= (CNTNAP1)	XP_024306779.1:p.Phe7=
NM_003632.3:c.19T= (CNTNAP1) MANE Select	NP_003623.1:p.Phe7=