Canonical Allele Identifier: CA2637988203
Gene: CCR10 HGNC NCBI
CNTNAP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42682528C>A , CM000679.2:g.42682528C>A GRCh38
NC_000017.10:g.40834546C>A , CM000679.1:g.40834546C>A GRCh37
NC_000017.9:g.38088072C>A NCBI36
NG_042091.1:g.4915C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000591568.1:c.-643+1288G>T (CCR10) ENSP00000467331.1:n.-643+1288G>T
ENST00000591765.1:c.-850G>T (CCR10) ENSP00000468135.1:n.-850G>T
XM_017025238.1:c.-302C>A (CNTNAP1) XP_016880727.1:n.-302C>A
XM_024451011.1:c.-302C>A (CNTNAP1) XP_024306779.1:n.-302C>A