Canonical Allele Identifier: CA2427988910
Gene: CFP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.47627601G= , CM000685.2:g.47627601G= GRCh38
NC_000023.10:g.47487000G= , CM000685.1:g.47487000G= GRCh37
NC_000023.9:g.47371944G= NCBI36
NG_009893.1:g.7705C= , LRG_129:g.7705C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000396992.8:c.444C= MANE Select ENSP00000380189.3:p.Cys148=
ENST00000640573.1:n.682C=
ENST00000247153.7:c.444C= ENSP00000247153.3:p.Cys148=
ENST00000377005.6:c.444C= ENSP00000366204.2:p.Cys148=
ENST00000396992.7:c.444C= ENSP00000380189.3:p.Cys148=
ENST00000469388.1:c.39C= ENSP00000418258.1:p.Cys13=
ENST00000485991.5:n.1741C=
NM_001145252.1:c.444C= NP_001138724.1:p.Cys148=
NM_002621.2:c.444C= , LRG_129t1:c.444C= NP_002612.1:p.Cys148=
XM_017029575.1:c.39C= XP_016885064.1:p.Cys13=
NM_001145252.3:c.444C= MANE Select NP_001138724.1:p.Cys148=