Canonical Allele Identifier: CA2637988322

Gene: CNTNAP1 CCR10

Linked Data

• gnomAD v4: 17-42682572-G-GAGGC

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42682575_42682576insCAGG , CM000679.2:g.42682575_42682576insCAGG	GRCh38
NC_000017.10:g.40834593_40834594insCAGG , CM000679.1:g.40834593_40834594insCAGG	GRCh37
NC_000017.9:g.38088119_38088120insCAGG	NCBI36
NG_042091.1:g.4962_4963insCAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264638.9:c.-255_-254insCAGG (CNTNAP1) MANE Select	ENSP00000264638.3:n.-255_-254insCAGG
ENST00000591568.1:c.-643+1243_-643+1244insGCCT (CCR10)	ENSP00000467331.1:n.-643+1243_-643+1244insGCCT
ENST00000591765.1:c.-895_-894insGCCT (CCR10)	ENSP00000468135.1:n.-895_-894insGCCT
XM_017025238.1:c.-255_-254insCAGG (CNTNAP1)	XP_016880727.1:n.-255_-254insCAGG
XM_024451011.1:c.-255_-254insCAGG (CNTNAP1)	XP_024306779.1:n.-255_-254insCAGG
NM_003632.3:c.-255_-254insCAGG (CNTNAP1) MANE Select	NP_003623.1:n.-255_-254insCAGG