Canonical Allele Identifier: CA2637988198
Gene: CCR10 HGNC NCBI
CNTNAP1 HGNC NCBI

Linked Data

gnomAD v4: 17-42682524-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42682524G>T , CM000679.2:g.42682524G>T GRCh38
NC_000017.10:g.40834542G>T , CM000679.1:g.40834542G>T GRCh37
NC_000017.9:g.38088068G>T NCBI36
NG_042091.1:g.4911G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000591568.1:c.-643+1292C>A (CCR10) ENSP00000467331.1:n.-643+1292C>A
ENST00000591765.1:c.-846C>A (CCR10) ENSP00000468135.1:n.-846C>A
XM_017025238.1:c.-306G>T (CNTNAP1) XP_016880727.1:n.-306G>T
XM_024451011.1:c.-306G>T (CNTNAP1) XP_024306779.1:n.-306G>T
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