Canonical Allele Identifier: CA2637988232

Gene: CNTNAP1 CCR10

Linked Data

• gnomAD v4: 17-42682544-G-GGCTCTCATCTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42682544_42682545insGCTCTCATCTTTT , CM000679.2:g.42682544_42682545insGCTCTCATCTTTT	GRCh38
NC_000017.10:g.40834562_40834563insGCTCTCATCTTTT , CM000679.1:g.40834562_40834563insGCTCTCATCTTTT	GRCh37
NC_000017.9:g.38088088_38088089insGCTCTCATCTTTT	NCBI36
NG_042091.1:g.4931_4932insGCTCTCATCTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264638.9:c.-286_-285insGCTCTCATCTTTT (CNTNAP1) MANE Select	ENSP00000264638.3:n.-286_-285insGCTCTCATCTTTT
ENST00000591568.1:c.-643+1271_-643+1272insAAAAGATGAGAGC (CCR10)	ENSP00000467331.1:n.-643+1271_-643+1272insAAAAGATGAGAGC
ENST00000591765.1:c.-867_-866insAAAAGATGAGAGC (CCR10)	ENSP00000468135.1:n.-867_-866insAAAAGATGAGAGC
XM_017025238.1:c.-286_-285insGCTCTCATCTTTT (CNTNAP1)	XP_016880727.1:n.-286_-285insGCTCTCATCTTTT
XM_024451011.1:c.-286_-285insGCTCTCATCTTTT (CNTNAP1)	XP_024306779.1:n.-286_-285insGCTCTCATCTTTT
NM_003632.3:c.-286_-285insGCTCTCATCTTTT (CNTNAP1) MANE Select	NP_003623.1:n.-286_-285insGCTCTCATCTTTT