Canonical Allele Identifier: CA571119415
Gene: CCDC170 HGNC NCBI

Linked Data

gnomAD v2: 6-151847669-T-TTTTTG
gnomAD v3: 6-151526534-T-TTTTTG
gnomAD v4: 6-151526534-T-TTTTTG
MyVariant Identifiers: chr6:g.151847670_151847671delinsTTTTGGA (hg19) chr6:g.151526535_151526536delinsTTTTGGA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151526534_151526535insTTTTG , CM000668.2:g.151526534_151526535insTTTTG GRCh38
NC_000006.11:g.151847669_151847670insTTTTG , CM000668.1:g.151847669_151847670insTTTTG GRCh37
NC_000006.10:g.151889362_151889363insTTTTG NCBI36
NG_021198.1:g.37495_37496insTTTTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000239374.8:c.58-9784_58-9783insTTTTG MANE Select ENSP00000239374.6:n.58-9784_58-9783insTTTTG
ENST00000239374.7:c.58-9784_58-9783insTTTTG ENSP00000239374.6:n.58-9784_58-9783insTTTTG
NM_025059.3:c.58-9784_58-9783insTTTTG NP_079335.2:n.58-9784_58-9783insTTTTG
NM_025059.4:c.58-9784_58-9783insTTTTG MANE Select NP_079335.2:n.58-9784_58-9783insTTTTG
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