Canonical Allele Identifier: CA2679936500
Gene: CCDC162P HGNC NCBI

Linked Data

gnomAD v4: 6-109305600-AAAGAAAAAG-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.109305612_109305620del , CM000668.2:g.109305612_109305620del GRCh38
NC_000006.11:g.109626815_109626823del , CM000668.1:g.109626815_109626823del GRCh37
NC_000006.10:g.109733508_109733516del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000429614.6:n.323-347_323-339del
ENST00000689724.1:n.55-347_55-339del
ENST00000691019.1:n.505-347_505-339del
ENST00000691264.1:n.61-347_61-339del
ENST00000693346.1:n.55-347_55-339del
ENST00000368966.10:n.4200-347_4200-339del
ENST00000638844.1:n.456-347_456-339del
ENST00000368966.8:n.456-347_456-339del
ENST00000422819.5:n.462-347_462-339del
ENST00000429614.5:n.323-347_323-339del
ENST00000615766.4:n.825-347_825-339del
NR_028595.1:n.323-347_323-339del
NR_152435.1:n.4168-347_4168-339del
Search 100 bp 5'
Search 100 bp 3'