Canonical Allele Identifier: CA817055292

Gene: CCDC162P

Linked Data

• dbSNP Id: rs1194342888
• gnomAD v3: 6-109305594-T-TA
• gnomAD v4: 6-109305594-T-TA
• MyVariant Identifiers: chr6:g.109626797_109626798insA (hg19) ; chr6:g.109305594_109305595insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.109305602dup , CM000668.2:g.109305602dup	GRCh38
NC_000006.11:g.109626805dup , CM000668.1:g.109626805dup	GRCh37
NC_000006.10:g.109733498dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000429614.6:n.323-357dup
ENST00000689724.1:n.55-357dup
ENST00000691019.1:n.505-357dup
ENST00000691264.1:n.61-357dup
ENST00000693346.1:n.55-357dup
ENST00000368966.10:n.4200-357dup
ENST00000638844.1:n.456-357dup
ENST00000368966.8:n.456-357dup
ENST00000422819.5:n.462-357dup
ENST00000429614.5:n.323-357dup
ENST00000615766.4:n.825-357dup
NR_028595.1:n.323-357dup
NR_152435.1:n.4168-357dup