Canonical Allele Identifier: CA2637988512
Gene: CNTNAP1 HGNC NCBI
CCR10 HGNC NCBI

Linked Data

gnomAD v4: 17-42682619-CGGAGGACCAGGAACCAGAGAGAGAGAGAGAGAAAAGA-C
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42682621_42682657del , CM000679.2:g.42682621_42682657del GRCh38
NC_000017.10:g.40834639_40834675del , CM000679.1:g.40834639_40834675del GRCh37
NC_000017.9:g.38088165_38088201del NCBI36
NG_042091.1:g.5008_5044del

Transcript Alleles

HGVS Amino-acid Change
ENST00000264638.9:c.-209_-173del (CNTNAP1) MANE Select ENSP00000264638.3:n.-209_-173del
ENST00000264638.8:c.-209_-173del (CNTNAP1) ENSP00000264638.3:n.-209_-173del
ENST00000591568.1:c.-643+1160_-643+1196del (CCR10) ENSP00000467331.1:n.-643+1160_-643+1196del
ENST00000591765.1:c.-978_-942del (CCR10) ENSP00000468135.1:n.-978_-942del
NM_003632.2:c.-209_-173del (CNTNAP1) NP_003623.1:n.-209_-173del
XM_017025238.1:c.-209_-173del (CNTNAP1) XP_016880727.1:n.-209_-173del
XM_024451011.1:c.-209_-173del (CNTNAP1) XP_024306779.1:n.-209_-173del
NM_003632.3:c.-209_-173del (CNTNAP1) MANE Select NP_003623.1:n.-209_-173del
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