Canonical Allele Identifier: CA2637988600

Gene: CNTNAP1 CCR10

Linked Data

• gnomAD v4: 17-42682634-C-CAGAGAGAGAGAGAGAGAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42682643_42682661dup , CM000679.2:g.42682643_42682661dup	GRCh38
NC_000017.10:g.40834661_40834679dup , CM000679.1:g.40834661_40834679dup	GRCh37
NC_000017.9:g.38088187_38088205dup	NCBI36
NG_042091.1:g.5030_5048dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264638.9:c.-187_-169dup (CNTNAP1) MANE Select	ENSP00000264638.3:n.-187_-169dup
ENST00000264638.8:c.-187_-169dup (CNTNAP1)	ENSP00000264638.3:n.-187_-169dup
ENST00000591568.1:c.-643+1163_-643+1181dup (CCR10)	ENSP00000467331.1:n.-643+1163_-643+1181dup
ENST00000591765.1:c.-975_-957dup (CCR10)	ENSP00000468135.1:n.-975_-957dup
NM_003632.2:c.-187_-169dup (CNTNAP1)	NP_003623.1:n.-187_-169dup
XM_017025238.1:c.-187_-169dup (CNTNAP1)	XP_016880727.1:n.-187_-169dup
XM_024451011.1:c.-187_-169dup (CNTNAP1)	XP_024306779.1:n.-187_-169dup
NM_003632.3:c.-187_-169dup (CNTNAP1) MANE Select	NP_003623.1:n.-187_-169dup