Canonical Allele Identifier: CA2637988735
Gene: CNTNAP1 HGNC NCBI
CCR10 HGNC NCBI

Linked Data

gnomAD v4: 17-42682669-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42682669A>T , CM000679.2:g.42682669A>T GRCh38
NC_000017.10:g.40834687A>T , CM000679.1:g.40834687A>T GRCh37
NC_000017.9:g.38088213A>T NCBI36
NG_042091.1:g.5056A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264638.9:c.-161A>T (CNTNAP1) MANE Select ENSP00000264638.3:n.-161A>T
ENST00000264638.8:c.-161A>T (CNTNAP1) ENSP00000264638.3:n.-161A>T
ENST00000591568.1:c.-643+1147T>A (CCR10) ENSP00000467331.1:n.-643+1147T>A
ENST00000591765.1:c.-991T>A (CCR10) ENSP00000468135.1:n.-991T>A
NM_003632.2:c.-161A>T (CNTNAP1) NP_003623.1:n.-161A>T
XM_005257748.4:c.-1181A>T (CNTNAP1) XP_005257805.1:n.-1181A>T
XM_017025238.1:c.-161A>T (CNTNAP1) XP_016880727.1:n.-161A>T
XM_024451011.1:c.-161A>T (CNTNAP1) XP_024306779.1:n.-161A>T
NM_003632.3:c.-161A>T (CNTNAP1) MANE Select NP_003623.1:n.-161A>T
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Search 100 bp 3'