Canonical Allele Identifier: CA2576277891

Gene: CNTNAP1 CCR10

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42682746del , CM000679.2:g.42682746del	GRCh38
NC_000017.10:g.40834764del , CM000679.1:g.40834764del	GRCh37
NC_000017.9:g.38088290del	NCBI36
NG_042091.1:g.5133del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264638.9:c.-84del (CNTNAP1) MANE Select	ENSP00000264638.3:n.-84del
ENST00000264638.8:c.-84del (CNTNAP1)	ENSP00000264638.3:n.-84del
ENST00000591568.1:c.-643+1070del (CCR10)	ENSP00000467331.1:n.-643+1070del
ENST00000591662.1:c.-84del (CNTNAP1)	ENSP00000466571.1:n.-84del
ENST00000591765.1:c.-1068del (CCR10)	ENSP00000468135.1:n.-1068del
NM_003632.2:c.-84del (CNTNAP1)	NP_003623.1:n.-84del
XM_005257748.4:c.-1104del (CNTNAP1)	XP_005257805.1:n.-1104del
XM_017025238.1:c.-84del (CNTNAP1)	XP_016880727.1:n.-84del
XM_024451011.1:c.-84del (CNTNAP1)	XP_024306779.1:n.-84del
NM_003632.3:c.-84del (CNTNAP1) MANE Select	NP_003623.1:n.-84del