Canonical Allele Identifier: CA2637988311

Gene: CNTNAP1 CCR10

Linked Data

• gnomAD v4: 17-42682570-G-GCTT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42682570_42682571insCTT , CM000679.2:g.42682570_42682571insCTT	GRCh38
NC_000017.10:g.40834588_40834589insCTT , CM000679.1:g.40834588_40834589insCTT	GRCh37
NC_000017.9:g.38088114_38088115insCTT	NCBI36
NG_042091.1:g.4957_4958insCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264638.9:c.-260_-259insCTT (CNTNAP1) MANE Select	ENSP00000264638.3:n.-260_-259insCTT
ENST00000591568.1:c.-643+1245_-643+1246insAAG (CCR10)	ENSP00000467331.1:n.-643+1245_-643+1246insAAG
ENST00000591765.1:c.-893_-892insAAG (CCR10)	ENSP00000468135.1:n.-893_-892insAAG
XM_017025238.1:c.-260_-259insCTT (CNTNAP1)	XP_016880727.1:n.-260_-259insCTT
XM_024451011.1:c.-260_-259insCTT (CNTNAP1)	XP_024306779.1:n.-260_-259insCTT
NM_003632.3:c.-260_-259insCTT (CNTNAP1) MANE Select	NP_003623.1:n.-260_-259insCTT