Canonical Allele Identifier: CA2260596148

Gene: CNTNAP1 CCR10

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42682828G= , CM000679.2:g.42682828G=	GRCh38
NC_000017.10:g.40834846G= , CM000679.1:g.40834846G=	GRCh37
NC_000017.9:g.38088372G=	NCBI36
NG_042091.1:g.5215G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264638.9:c.-2G= (CNTNAP1) MANE Select	ENSP00000264638.3:n.-2G=
ENST00000264638.8:c.-2G= (CNTNAP1)	ENSP00000264638.3:n.-2G=
ENST00000591568.1:c.-643+988C= (CCR10)	ENSP00000467331.1:n.-643+988C=
ENST00000591662.1:c.-2G= (CNTNAP1)	ENSP00000466571.1:n.-2G=
ENST00000591765.1:c.-1150C= (CCR10)	ENSP00000468135.1:n.-1150C=
NM_003632.2:c.-2G= (CNTNAP1)	NP_003623.1:n.-2G=
XM_005257748.4:c.-1022G= (CNTNAP1)	XP_005257805.1:n.-1022G=
XM_017025238.1:c.-2G= (CNTNAP1)	XP_016880727.1:n.-2G=
XM_024451011.1:c.-2G= (CNTNAP1)	XP_024306779.1:n.-2G=
NM_003632.3:c.-2G= (CNTNAP1) MANE Select	NP_003623.1:n.-2G=