Canonical Allele Identifier: CA2260596062
Gene: CNTNAP1 HGNC NCBI
CCR10 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42682667A= , CM000679.2:g.42682667A= GRCh38
NC_000017.10:g.40834685A= , CM000679.1:g.40834685A= GRCh37
NC_000017.9:g.38088211A= NCBI36
NG_042091.1:g.5054A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264638.9:c.-163A= (CNTNAP1) MANE Select ENSP00000264638.3:n.-163A=
ENST00000264638.8:c.-163A= (CNTNAP1) ENSP00000264638.3:n.-163A=
ENST00000591568.1:c.-643+1149T= (CCR10) ENSP00000467331.1:n.-643+1149T=
ENST00000591765.1:c.-989T= (CCR10) ENSP00000468135.1:n.-989T=
NM_003632.2:c.-163A= (CNTNAP1) NP_003623.1:n.-163A=
XM_005257748.4:c.-1183A= (CNTNAP1) XP_005257805.1:n.-1183A=
XM_017025238.1:c.-163A= (CNTNAP1) XP_016880727.1:n.-163A=
XM_024451011.1:c.-163A= (CNTNAP1) XP_024306779.1:n.-163A=
NM_003632.3:c.-163A= (CNTNAP1) MANE Select NP_003623.1:n.-163A=
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