Canonical Allele Identifier: CA290788964
Gene: CNTNAP1 HGNC NCBI
CCR10 HGNC NCBI

Linked Data

dbSNP Id: rs975186796
gnomAD v3: 17-42682534-A-T
gnomAD v4: 17-42682534-A-T
MyVariant Identifiers: chr17:g.40834552A>T (hg19) chr17:g.42682534A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42682534A>T , CM000679.2:g.42682534A>T GRCh38
NC_000017.10:g.40834552A>T , CM000679.1:g.40834552A>T GRCh37
NC_000017.9:g.38088078A>T NCBI36
NG_042091.1:g.4921A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264638.9:c.-296A>T (CNTNAP1) MANE Select ENSP00000264638.3:n.-296A>T
ENST00000591568.1:c.-643+1282T>A (CCR10) ENSP00000467331.1:n.-643+1282T>A
ENST00000591765.1:c.-856T>A (CCR10) ENSP00000468135.1:n.-856T>A
XM_017025238.1:c.-296A>T (CNTNAP1) XP_016880727.1:n.-296A>T
XM_024451011.1:c.-296A>T (CNTNAP1) XP_024306779.1:n.-296A>T
NM_003632.3:c.-296A>T (CNTNAP1) MANE Select NP_003623.1:n.-296A>T
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