Canonical Allele Identifier: CA2637988205
Gene: CCR10 HGNC NCBI
CNTNAP1 HGNC NCBI

Linked Data

gnomAD v4: 17-42682528-C-T
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Genomic Alleles

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

Transcript Alleles

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