Canonical Allele Identifier: CA817055245
Gene: CCDC162P HGNC NCBI

Linked Data

dbSNP Id: rs1189499012

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.109305445_109305449del , CM000668.2:g.109305445_109305449del GRCh38
NC_000006.11:g.109626648_109626652del , CM000668.1:g.109626648_109626652del GRCh37
NC_000006.10:g.109733341_109733345del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000429614.6:n.323-514_323-510del
ENST00000689724.1:n.55-514_55-510del
ENST00000691019.1:n.505-514_505-510del
ENST00000691264.1:n.61-514_61-510del
ENST00000693346.1:n.55-514_55-510del
ENST00000368966.10:n.4200-514_4200-510del
ENST00000638844.1:n.456-514_456-510del
ENST00000368966.8:n.456-514_456-510del
ENST00000422819.5:n.462-514_462-510del
ENST00000429614.5:n.323-514_323-510del
ENST00000615766.4:n.825-514_825-510del
NR_028595.1:n.323-514_323-510del
NR_152435.1:n.4168-514_4168-510del