Canonical Allele Identifier: CA2679936583
Gene: CCDC162P HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.109305712del , CM000668.2:g.109305712del GRCh38
NC_000006.11:g.109626915del , CM000668.1:g.109626915del GRCh37
NC_000006.10:g.109733608del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000429614.6:n.323-247del
ENST00000689724.1:n.55-247del
ENST00000691019.1:n.505-247del
ENST00000691264.1:n.61-247del
ENST00000693346.1:n.55-247del
ENST00000368966.10:n.4200-247del
ENST00000638844.1:n.456-247del
ENST00000368966.8:n.456-247del
ENST00000422819.5:n.462-247del
ENST00000429614.5:n.323-247del
ENST00000615766.4:n.825-247del
NR_028595.1:n.323-247del
NR_152435.1:n.4168-247del