Canonical Allele Identifier: CA817055435

Gene: CCDC162P

Linked Data

• dbSNP Id: rs1182547868
• gnomAD v3: 6-109305853-T-TTAA
• gnomAD v4: 6-109305853-T-TTAA
• MyVariant Identifiers: chr6:g.109627056_109627057insTAA (hg19) ; chr6:g.109305853_109305854insTAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.109305856_109305858dup , CM000668.2:g.109305856_109305858dup	GRCh38
NC_000006.11:g.109627059_109627061dup , CM000668.1:g.109627059_109627061dup	GRCh37
NC_000006.10:g.109733752_109733754dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000429614.6:n.323-103_323-101dup
ENST00000689724.1:n.55-103_55-101dup
ENST00000691019.1:n.505-103_505-101dup
ENST00000691264.1:n.61-103_61-101dup
ENST00000693346.1:n.55-103_55-101dup
ENST00000368966.10:n.4200-103_4200-101dup
ENST00000638844.1:n.456-103_456-101dup
ENST00000368966.8:n.456-103_456-101dup
ENST00000422819.5:n.462-103_462-101dup
ENST00000429614.5:n.323-103_323-101dup
ENST00000615766.4:n.825-103_825-101dup
NR_028595.1:n.323-103_323-101dup
NR_152435.1:n.4168-103_4168-101dup