Canonical Allele Identifier: CA3951358

Gene: CCDC162P

Linked Data

• dbSNP Id: rs755457073
• ExAC: 6:109627123 TA / T
• gnomAD v2: 6-109627123-TA-T
• gnomAD v3: 6-109305920-TA-T
• gnomAD v4: 6-109305920-TA-T
• MyVariant Identifiers: chr6:g.109627124del (hg19) ; chr6:g.109305921del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.109305922del , CM000668.2:g.109305922del	GRCh38
NC_000006.11:g.109627125del , CM000668.1:g.109627125del	GRCh37
NC_000006.10:g.109733818del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000429614.6:n.323-37del
ENST00000689724.1:n.55-37del
ENST00000691019.1:n.505-37del
ENST00000691264.1:n.61-37del
ENST00000693346.1:n.55-37del
ENST00000368966.10:n.4200-37del
ENST00000638844.1:n.456-37del
ENST00000368966.8:n.456-37del
ENST00000422819.5:n.462-37del
ENST00000429614.5:n.323-37del
ENST00000615766.4:n.825-37del
NR_028595.1:n.323-37del
NR_152435.1:n.4168-37del