Canonical Allele Identifier: CA2637988266

Gene: CNTNAP1 CCR10

Linked Data

• gnomAD v4: 17-42682560-TGGGGAAG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42682565_42682571del , CM000679.2:g.42682565_42682571del	GRCh38
NC_000017.10:g.40834583_40834589del , CM000679.1:g.40834583_40834589del	GRCh37
NC_000017.9:g.38088109_38088115del	NCBI36
NG_042091.1:g.4952_4958del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264638.9:c.-265_-259del (CNTNAP1) MANE Select	ENSP00000264638.3:n.-265_-259del
ENST00000591568.1:c.-643+1249_-643+1255del (CCR10)	ENSP00000467331.1:n.-643+1249_-643+1255del
ENST00000591765.1:c.-889_-883del (CCR10)	ENSP00000468135.1:n.-889_-883del
XM_017025238.1:c.-265_-259del (CNTNAP1)	XP_016880727.1:n.-265_-259del
XM_024451011.1:c.-265_-259del (CNTNAP1)	XP_024306779.1:n.-265_-259del
NM_003632.3:c.-265_-259del (CNTNAP1) MANE Select	NP_003623.1:n.-265_-259del