Canonical Allele Identifier: CA2557018786
Gene: CCDC162P HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.109305308_109305309insT , CM000668.2:g.109305308_109305309insT GRCh38
NC_000006.11:g.109626511_109626512insT , CM000668.1:g.109626511_109626512insT GRCh37
NC_000006.10:g.109733204_109733205insT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000429614.6:n.323-651_323-650insT
ENST00000689724.1:n.55-651_55-650insT
ENST00000691019.1:n.505-651_505-650insT
ENST00000691264.1:n.61-651_61-650insT
ENST00000693346.1:n.55-651_55-650insT
ENST00000368966.10:n.4200-651_4200-650insT
ENST00000638844.1:n.456-651_456-650insT
ENST00000368966.8:n.456-651_456-650insT
ENST00000422819.5:n.462-651_462-650insT
ENST00000429614.5:n.323-651_323-650insT
ENST00000615766.4:n.825-651_825-650insT
NR_028595.1:n.323-651_323-650insT
NR_152435.1:n.4168-651_4168-650insT