Canonical Allele Identifier: CA2712661929

Gene: CCDC162P

Linked Data

• dbSNP Id: rs2115089181

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.109305463_109305465del , CM000668.2:g.109305463_109305465del	GRCh38
NC_000006.11:g.109626666_109626668del , CM000668.1:g.109626666_109626668del	GRCh37
NC_000006.10:g.109733359_109733361del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000429614.6:n.323-496_323-494del
ENST00000689724.1:n.55-496_55-494del
ENST00000691019.1:n.505-496_505-494del
ENST00000691264.1:n.61-496_61-494del
ENST00000693346.1:n.55-496_55-494del
ENST00000368966.10:n.4200-496_4200-494del
ENST00000638844.1:n.456-496_456-494del
ENST00000368966.8:n.456-496_456-494del
ENST00000422819.5:n.462-496_462-494del
ENST00000429614.5:n.323-496_323-494del
ENST00000615766.4:n.825-496_825-494del
NR_028595.1:n.323-496_323-494del
NR_152435.1:n.4168-496_4168-494del