Canonical Allele Identifier: CA493112015

Gene: CCNF

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2435666_2435681del , CM000678.2:g.2435666_2435681del	GRCh38
NC_000016.9:g.2485667_2485682del , CM000678.1:g.2485667_2485682del	GRCh37
NC_000016.8:g.2425668_2425683del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001761.3:c.279-140_279-125del MANE Select	NP_001752.2:n.279-140_279-125del
ENST00000397066.9:c.279-140_279-125del MANE Select	ENSP00000380256.4:n.279-140_279-125del
NM_001323538.1:c.-646-140_-646-125del	NP_001310467.1:n.-646-140_-646-125del
NM_001323538.2:c.-646-140_-646-125del	NP_001310467.1:n.-646-140_-646-125del
NM_001761.2:c.279-140_279-125del	NP_001752.2:n.279-140_279-125del
ENST00000293968.11:c.172-140_172-125del	ENSP00000293968.7:n.172-140_172-125del
ENST00000397066.8:c.279-140_279-125del	ENSP00000380256.4:n.279-140_279-125del
ENST00000569093.1:n.312-140_312-125del