Canonical Allele Identifier: CA2497169108

Gene: CCDC162P

Linked Data

• dbSNP Id: rs1776652537

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.109305934_109305946del , CM000668.2:g.109305934_109305946del	GRCh38
NC_000006.11:g.109627137_109627149del , CM000668.1:g.109627137_109627149del	GRCh37
NC_000006.10:g.109733830_109733842del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000429614.6:n.323-25_323-13del
ENST00000689724.1:n.55-25_55-13del
ENST00000691019.1:n.505-25_505-13del
ENST00000691264.1:n.61-25_61-13del
ENST00000693346.1:n.55-25_55-13del
ENST00000368966.10:n.4200-25_4200-13del
ENST00000638844.1:n.456-25_456-13del
ENST00000368966.8:n.456-25_456-13del
ENST00000422819.5:n.462-25_462-13del
ENST00000429614.5:n.323-25_323-13del
ENST00000615766.4:n.825-25_825-13del
NR_028595.1:n.323-25_323-13del
NR_152435.1:n.4168-25_4168-13del