Canonical Allele Identifier: CA290788986
Gene: CNTNAP1 HGNC NCBI
CCR10 HGNC NCBI

Linked Data

dbSNP Id: rs893687268
gnomAD v4: 17-42682568-G-T
MyVariant Identifiers: chr17:g.40834586G>T (hg19) chr17:g.42682568G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42682568G>T , CM000679.2:g.42682568G>T GRCh38
NC_000017.10:g.40834586G>T , CM000679.1:g.40834586G>T GRCh37
NC_000017.9:g.38088112G>T NCBI36
NG_042091.1:g.4955G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264638.9:c.-262G>T (CNTNAP1) MANE Select ENSP00000264638.3:n.-262G>T
ENST00000591568.1:c.-643+1248C>A (CCR10) ENSP00000467331.1:n.-643+1248C>A
ENST00000591765.1:c.-890C>A (CCR10) ENSP00000468135.1:n.-890C>A
XM_017025238.1:c.-262G>T (CNTNAP1) XP_016880727.1:n.-262G>T
XM_024451011.1:c.-262G>T (CNTNAP1) XP_024306779.1:n.-262G>T
NM_003632.3:c.-262G>T (CNTNAP1) MANE Select NP_003623.1:n.-262G>T
Search 100 bp 5'
Search 100 bp 3'