Canonical Allele Identifier: CA2837998374
Gene: CCDC162P HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.109313625A= , CM000668.2:g.109313625A= GRCh38
NC_000006.11:g.109634828A= , CM000668.1:g.109634828A= GRCh37
NC_000006.10:g.109741521A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000689724.1:n.621-438A=
ENST00000691019.1:n.908-438A=
ENST00000691264.1:n.464-438A=
ENST00000368966.10:n.4603-438A=
ENST00000638844.1:n.859-438A=
ENST00000368966.8:n.859-438A=
ENST00000506861.1:n.348+3971A=
ENST00000508210.1:n.386-438A=
NR_152435.1:n.4571-438A=