Canonical Allele Identifier: CA2579597275
Gene: CFP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.47627645del , CM000685.2:g.47627645del GRCh38
NC_000023.10:g.47487044del , CM000685.1:g.47487044del GRCh37
NC_000023.9:g.47371988del NCBI36
NG_009893.1:g.7661del , LRG_129:g.7661del

Transcript Alleles

HGVS Amino-acid Change
ENST00000396992.8:c.404-4del MANE Select ENSP00000380189.3:n.404-4del
ENST00000640573.1:n.642-4del
ENST00000247153.7:c.404-4del ENSP00000247153.3:n.404-4del
ENST00000377005.6:c.404-4del ENSP00000366204.2:n.404-4del
ENST00000396992.7:c.404-4del ENSP00000380189.3:n.404-4del
ENST00000469388.1:c.-2-4del ENSP00000418258.1:n.-2-4del
ENST00000485991.5:n.1701-4del
NM_001145252.1:c.404-4del NP_001138724.1:n.404-4del
NM_002621.2:c.404-4del , LRG_129t1:c.404-4del NP_002612.1:n.404-4del
XM_017029575.1:c.-2-4del XP_016885064.1:n.-2-4del
NM_001145252.3:c.404-4del MANE Select NP_001138724.1:n.404-4del