Canonical Allele Identifier: CA2820776305
Gene: CFP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.47627680del , CM000685.2:g.47627680del GRCh38
NC_000023.10:g.47487079del , CM000685.1:g.47487079del GRCh37
NC_000023.9:g.47372023del NCBI36
NG_009893.1:g.7629del , LRG_129:g.7629del

Transcript Alleles

HGVS Amino-acid Change
ENST00000396992.8:c.404-36del MANE Select ENSP00000380189.3:n.404-36del
ENST00000640573.1:n.642-36del
ENST00000247153.7:c.404-36del ENSP00000247153.3:n.404-36del
ENST00000377005.6:c.404-36del ENSP00000366204.2:n.404-36del
ENST00000396992.7:c.404-36del ENSP00000380189.3:n.404-36del
ENST00000469388.1:c.-2-36del ENSP00000418258.1:n.-2-36del
ENST00000485991.5:n.1701-36del
NM_001145252.1:c.404-36del NP_001138724.1:n.404-36del
NM_002621.2:c.404-36del , LRG_129t1:c.404-36del NP_002612.1:n.404-36del
XM_017029575.1:c.-2-36del XP_016885064.1:n.-2-36del
NM_001145252.3:c.404-36del MANE Select NP_001138724.1:n.404-36del
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