Canonical Allele Identifier: CA2260596027
Gene: CNTNAP1 HGNC NCBI
CCR10 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42682613G= , CM000679.2:g.42682613G= GRCh38
NC_000017.10:g.40834631G= , CM000679.1:g.40834631G= GRCh37
NC_000017.9:g.38088157G= NCBI36
NG_042091.1:g.5000G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264638.9:c.-217G= (CNTNAP1) MANE Select ENSP00000264638.3:n.-217G=
ENST00000264638.8:c.-217G= (CNTNAP1) ENSP00000264638.3:n.-217G=
ENST00000591568.1:c.-643+1203C= (CCR10) ENSP00000467331.1:n.-643+1203C=
ENST00000591765.1:c.-935C= (CCR10) ENSP00000468135.1:n.-935C=
XM_017025238.1:c.-217G= (CNTNAP1) XP_016880727.1:n.-217G=
XM_024451011.1:c.-217G= (CNTNAP1) XP_024306779.1:n.-217G=
NM_003632.3:c.-217G= (CNTNAP1) MANE Select NP_003623.1:n.-217G=
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