Canonical Allele Identifier: CA2507823630

Gene: CCDC162P

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.109305309_109305310insCCAT , CM000668.2:g.109305309_109305310insCCAT	GRCh38
NC_000006.11:g.109626512_109626513insCCAT , CM000668.1:g.109626512_109626513insCCAT	GRCh37
NC_000006.10:g.109733205_109733206insCCAT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000429614.6:n.323-650_323-649insCCAT
ENST00000689724.1:n.55-650_55-649insCCAT
ENST00000691019.1:n.505-650_505-649insCCAT
ENST00000691264.1:n.61-650_61-649insCCAT
ENST00000693346.1:n.55-650_55-649insCCAT
ENST00000368966.10:n.4200-650_4200-649insCCAT
ENST00000638844.1:n.456-650_456-649insCCAT
ENST00000368966.8:n.456-650_456-649insCCAT
ENST00000422819.5:n.462-650_462-649insCCAT
ENST00000429614.5:n.323-650_323-649insCCAT
ENST00000615766.4:n.825-650_825-649insCCAT
NR_028595.1:n.323-650_323-649insCCAT
NR_152435.1:n.4168-650_4168-649insCCAT