Canonical Allele Identifier: CA2637988235

Gene: CNTNAP1 CCR10

Linked Data

• gnomAD v4: 17-42682545-C-CCT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42682546_42682547insTC , CM000679.2:g.42682546_42682547insTC	GRCh38
NC_000017.10:g.40834564_40834565insTC , CM000679.1:g.40834564_40834565insTC	GRCh37
NC_000017.9:g.38088090_38088091insTC	NCBI36
NG_042091.1:g.4933_4934insTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264638.9:c.-284_-283insTC (CNTNAP1) MANE Select	ENSP00000264638.3:n.-284_-283insTC
ENST00000591568.1:c.-643+1270_-643+1271insAG (CCR10)	ENSP00000467331.1:n.-643+1270_-643+1271insAG
ENST00000591765.1:c.-868_-867insAG (CCR10)	ENSP00000468135.1:n.-868_-867insAG
XM_017025238.1:c.-284_-283insTC (CNTNAP1)	XP_016880727.1:n.-284_-283insTC
XM_024451011.1:c.-284_-283insTC (CNTNAP1)	XP_024306779.1:n.-284_-283insTC
NM_003632.3:c.-284_-283insTC (CNTNAP1) MANE Select	NP_003623.1:n.-284_-283insTC