Canonical Allele Identifier: CA2637988206
Gene: CCR10 HGNC NCBI
CNTNAP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42682529G>A , CM000679.2:g.42682529G>A GRCh38
NC_000017.10:g.40834547G>A , CM000679.1:g.40834547G>A GRCh37
NC_000017.9:g.38088073G>A NCBI36
NG_042091.1:g.4916G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000591568.1:c.-643+1287C>T (CCR10) ENSP00000467331.1:n.-643+1287C>T
ENST00000591765.1:c.-851C>T (CCR10) ENSP00000468135.1:n.-851C>T
XM_017025238.1:c.-301G>A (CNTNAP1) XP_016880727.1:n.-301G>A
XM_024451011.1:c.-301G>A (CNTNAP1) XP_024306779.1:n.-301G>A