Canonical Allele Identifier: CA772111933
Gene: CNTNAP1 HGNC NCBI
CCR10 HGNC NCBI

Linked Data

dbSNP Id: rs1441624568
gnomAD v3: 17-42682583-A-G
gnomAD v4: 17-42682583-A-G
MyVariant Identifiers: chr17:g.40834601A>G (hg19) chr17:g.42682583A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42682583A>G , CM000679.2:g.42682583A>G GRCh38
NC_000017.10:g.40834601A>G , CM000679.1:g.40834601A>G GRCh37
NC_000017.9:g.38088127A>G NCBI36
NG_042091.1:g.4970A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264638.9:c.-247A>G (CNTNAP1) MANE Select ENSP00000264638.3:n.-247A>G
ENST00000591568.1:c.-643+1233T>C (CCR10) ENSP00000467331.1:n.-643+1233T>C
ENST00000591765.1:c.-905T>C (CCR10) ENSP00000468135.1:n.-905T>C
XM_017025238.1:c.-247A>G (CNTNAP1) XP_016880727.1:n.-247A>G
XM_024451011.1:c.-247A>G (CNTNAP1) XP_024306779.1:n.-247A>G
NM_003632.3:c.-247A>G (CNTNAP1) MANE Select NP_003623.1:n.-247A>G
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