Canonical Allele Identifier: CA2637988660

Gene: CNTNAP1 CCR10

Linked Data

• gnomAD v4: 17-42682647-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42682648del , CM000679.2:g.42682648del	GRCh38
NC_000017.10:g.40834666del , CM000679.1:g.40834666del	GRCh37
NC_000017.9:g.38088192del	NCBI36
NG_042091.1:g.5035del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264638.9:c.-182del (CNTNAP1) MANE Select	ENSP00000264638.3:n.-182del
ENST00000264638.8:c.-182del (CNTNAP1)	ENSP00000264638.3:n.-182del
ENST00000591568.1:c.-643+1168del (CCR10)	ENSP00000467331.1:n.-643+1168del
ENST00000591765.1:c.-970del (CCR10)	ENSP00000468135.1:n.-970del
NM_003632.2:c.-182del (CNTNAP1)	NP_003623.1:n.-182del
XM_005257748.4:c.-1202del (CNTNAP1)	XP_005257805.1:n.-1202del
XM_017025238.1:c.-182del (CNTNAP1)	XP_016880727.1:n.-182del
XM_024451011.1:c.-182del (CNTNAP1)	XP_024306779.1:n.-182del
NM_003632.3:c.-182del (CNTNAP1) MANE Select	NP_003623.1:n.-182del