Canonical Allele Identifier: CA451867405

Gene: CCDC162P

Linked Data

• MyVariant Identifiers: chr6:g.109626788A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.109305585A>C , CM000668.2:g.109305585A>C	GRCh38
NC_000006.11:g.109626788A>C , CM000668.1:g.109626788A>C	GRCh37
NC_000006.10:g.109733481A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000429614.6:n.323-374A>C
ENST00000689724.1:n.55-374A>C
ENST00000691019.1:n.505-374A>C
ENST00000691264.1:n.61-374A>C
ENST00000693346.1:n.55-374A>C
ENST00000368966.10:n.4200-374A>C
ENST00000638844.1:n.456-374A>C
ENST00000368966.8:n.456-374A>C
ENST00000422819.5:n.462-374A>C
ENST00000429614.5:n.323-374A>C
ENST00000615766.4:n.825-374A>C
NR_028595.1:n.323-374A>C
NR_152435.1:n.4168-374A>C