Canonical Allele Identifier: CA1093027051

Gene: CCDC162P

Linked Data

• dbSNP Id: rs1776647722
• gnomAD v3: 6-109305558-CT-C
• gnomAD v4: 6-109305558-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.109305561del , CM000668.2:g.109305561del	GRCh38
NC_000006.11:g.109626764del , CM000668.1:g.109626764del	GRCh37
NC_000006.10:g.109733457del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000429614.6:n.323-398del
ENST00000689724.1:n.55-398del
ENST00000691019.1:n.505-398del
ENST00000691264.1:n.61-398del
ENST00000693346.1:n.55-398del
ENST00000368966.10:n.4200-398del
ENST00000638844.1:n.456-398del
ENST00000368966.8:n.456-398del
ENST00000422819.5:n.462-398del
ENST00000429614.5:n.323-398del
ENST00000615766.4:n.825-398del
NR_028595.1:n.323-398del
NR_152435.1:n.4168-398del