Canonical Allele Identifier: CA2637988432

Gene: CNTNAP1 CCR10

Linked Data

• gnomAD v4: 17-42682605-TAGAGAGAGAAGAGCGGAGGACCAGGAACCAGAGAGAG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42682616_42682652del , CM000679.2:g.42682616_42682652del	GRCh38
NC_000017.10:g.40834634_40834670del , CM000679.1:g.40834634_40834670del	GRCh37
NC_000017.9:g.38088160_38088196del	NCBI36
NG_042091.1:g.5003_5039del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264638.9:c.-214_-178del (CNTNAP1) MANE Select	ENSP00000264638.3:n.-214_-178del
ENST00000591568.1:c.-643+1174_-643+1210del (CCR10)	ENSP00000467331.1:n.-643+1174_-643+1210del
ENST00000591765.1:c.-964_-928del (CCR10)	ENSP00000468135.1:n.-964_-928del
XM_017025238.1:c.-214_-178del (CNTNAP1)	XP_016880727.1:n.-214_-178del
XM_024451011.1:c.-214_-178del (CNTNAP1)	XP_024306779.1:n.-214_-178del
NM_003632.3:c.-214_-178del (CNTNAP1) MANE Select	NP_003623.1:n.-214_-178del