Canonical Allele Identifier: CA412838660
Gene: CFP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.47627542G>C , CM000685.2:g.47627542G>C GRCh38
NC_000023.10:g.47486941G>C , CM000685.1:g.47486941G>C GRCh37
NC_000023.9:g.47371885G>C NCBI36
NG_009893.1:g.7764C>G , LRG_129:g.7764C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000396992.8:c.503C>G MANE Select ENSP00000380189.3:p.Pro168Arg
ENST00000640573.1:n.741C>G
ENST00000247153.7:c.503C>G ENSP00000247153.3:p.Pro168Arg
ENST00000377005.6:c.503C>G ENSP00000366204.2:p.Pro168Arg
ENST00000396992.7:c.503C>G ENSP00000380189.3:p.Pro168Arg
ENST00000469388.1:c.98C>G ENSP00000418258.1:p.Pro33Arg
ENST00000485991.5:n.1800C>G
NM_001145252.1:c.503C>G NP_001138724.1:p.Pro168Arg
NM_002621.2:c.503C>G , LRG_129t1:c.503C>G NP_002612.1:p.Pro168Arg
XM_017029575.1:c.98C>G XP_016885064.1:p.Pro33Arg
NM_001145252.3:c.503C>G MANE Select NP_001138724.1:p.Pro168Arg