Canonical Allele Identifier: CA2260596150

Gene: CNTNAP1 CCR10

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42682830A= , CM000679.2:g.42682830A=	GRCh38
NC_000017.10:g.40834848A= , CM000679.1:g.40834848A=	GRCh37
NC_000017.9:g.38088374A=	NCBI36
NG_042091.1:g.5217A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264638.9:c.1A= (CNTNAP1) MANE Select	ENSP00000264638.3:p.Met1=
ENST00000264638.8:c.1A= (CNTNAP1)	ENSP00000264638.3:p.Met1=
ENST00000591568.1:c.-643+986T= (CCR10)	ENSP00000467331.1:n.-643+986T=
ENST00000591662.1:c.1A= (CNTNAP1)	ENSP00000466571.1:p.Met1=
ENST00000591765.1:c.-1152T= (CCR10)	ENSP00000468135.1:n.-1152T=
NM_003632.2:c.1A= (CNTNAP1)	NP_003623.1:p.Met1=
XM_005257748.4:c.-1020A= (CNTNAP1)	XP_005257805.1:n.-1020A=
XM_017025238.1:c.1A= (CNTNAP1)	XP_016880727.1:p.Met1=
XM_024451011.1:c.1A= (CNTNAP1)	XP_024306779.1:p.Met1=
NM_003632.3:c.1A= (CNTNAP1) MANE Select	NP_003623.1:p.Met1=