Canonical Allele Identifier: CA451867165

Gene: CCDC162P

Linked Data

• MyVariant Identifiers: chr6:g.109626707A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.109305504A>T , CM000668.2:g.109305504A>T	GRCh38
NC_000006.11:g.109626707A>T , CM000668.1:g.109626707A>T	GRCh37
NC_000006.10:g.109733400A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000429614.6:n.323-455A>T
ENST00000689724.1:n.55-455A>T
ENST00000691019.1:n.505-455A>T
ENST00000691264.1:n.61-455A>T
ENST00000693346.1:n.55-455A>T
ENST00000368966.10:n.4200-455A>T
ENST00000638844.1:n.456-455A>T
ENST00000368966.8:n.456-455A>T
ENST00000422819.5:n.462-455A>T
ENST00000429614.5:n.323-455A>T
ENST00000615766.4:n.825-455A>T
NR_028595.1:n.323-455A>T
NR_152435.1:n.4168-455A>T