Canonical Allele Identifier: CA2679936498
Gene: CCDC162P HGNC NCBI

Linked Data

gnomAD v4: 6-109305593-T-TA
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.109305593_109305594insA , CM000668.2:g.109305593_109305594insA GRCh38
NC_000006.11:g.109626796_109626797insA , CM000668.1:g.109626796_109626797insA GRCh37
NC_000006.10:g.109733489_109733490insA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000429614.6:n.323-366_323-365insA
ENST00000689724.1:n.55-366_55-365insA
ENST00000691019.1:n.505-366_505-365insA
ENST00000691264.1:n.61-366_61-365insA
ENST00000693346.1:n.55-366_55-365insA
ENST00000368966.10:n.4200-366_4200-365insA
ENST00000638844.1:n.456-366_456-365insA
ENST00000368966.8:n.456-366_456-365insA
ENST00000422819.5:n.462-366_462-365insA
ENST00000429614.5:n.323-366_323-365insA
ENST00000615766.4:n.825-366_825-365insA
NR_028595.1:n.323-366_323-365insA
NR_152435.1:n.4168-366_4168-365insA
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