Canonical Allele Identifier: CA145763369
Gene: CCDC162P HGNC NCBI

Linked Data

dbSNP Id: rs575155369

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.109305760_109305770del , CM000668.2:g.109305760_109305770del GRCh38
NC_000006.11:g.109626963_109626973del , CM000668.1:g.109626963_109626973del GRCh37
NC_000006.10:g.109733656_109733666del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000429614.6:n.323-199_323-189del
ENST00000689724.1:n.55-199_55-189del
ENST00000691019.1:n.505-199_505-189del
ENST00000691264.1:n.61-199_61-189del
ENST00000693346.1:n.55-199_55-189del
ENST00000368966.10:n.4200-199_4200-189del
ENST00000638844.1:n.456-199_456-189del
ENST00000368966.8:n.456-199_456-189del
ENST00000422819.5:n.462-199_462-189del
ENST00000429614.5:n.323-199_323-189del
ENST00000615766.4:n.825-199_825-189del
NR_028595.1:n.323-199_323-189del
NR_152435.1:n.4168-199_4168-189del