Canonical Allele Identifier: CA4051996
Gene: CCDC170 HGNC NCBI

Linked Data

dbSNP Id: rs751612825
ExAC: 6:151936774 T / TA
gnomAD v2: 6-151936774-T-TA
gnomAD v3: 6-151615639-T-TA
gnomAD v4: 6-151615639-T-TA
COSMIC: COSM1441223
MyVariant Identifiers: chr6:g.151936775_151936776insA (hg19) chr6:g.151936774_151936775insA (hg19) chr6:g.151615640_151615641insA (hg38) chr6:g.151615639_151615640insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151615646dup , CM000668.2:g.151615646dup GRCh38
NC_000006.11:g.151936781dup , CM000668.1:g.151936781dup GRCh37
NC_000006.10:g.151978474dup NCBI36
NG_021198.1:g.126607dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000239374.8:c.1914dup MANE Select ENSP00000239374.6:p.Ser639IlefsTer?
ENST00000239374.7:c.1914dup ENSP00000239374.6:p.Ser639IlefsTer?
NM_025059.3:c.1914dup NP_079335.2:p.Ser639IlefsTer?
XM_011536147.1:c.1932dup XP_011534449.1:p.Ser645IlefsTer?
XM_011536148.1:c.1731dup XP_011534450.1:p.Ser578IlefsTer?
XM_011536147.2:c.1932dup XP_011534449.1:p.Ser645IlefsTer?
XM_011536148.2:c.1731dup XP_011534450.1:p.Ser578IlefsTer?
XR_001743865.1:n.129+1081dup
NM_025059.4:c.1914dup MANE Select NP_079335.2:p.Ser639IlefsTer?
Search 100 bp 5'
Search 100 bp 3'