Canonical Allele Identifier: CA412838857
Gene: CFP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.47627633C>G , CM000685.2:g.47627633C>G GRCh38
NC_000023.10:g.47487032C>G , CM000685.1:g.47487032C>G GRCh37
NC_000023.9:g.47371976C>G NCBI36
NG_009893.1:g.7673G>C , LRG_129:g.7673G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000396992.8:c.412G>C MANE Select ENSP00000380189.3:p.Gly138Arg
ENST00000640573.1:n.650G>C
ENST00000247153.7:c.412G>C ENSP00000247153.3:p.Gly138Arg
ENST00000377005.6:c.412G>C ENSP00000366204.2:p.Gly138Arg
ENST00000396992.7:c.412G>C ENSP00000380189.3:p.Gly138Arg
ENST00000469388.1:c.7G>C ENSP00000418258.1:p.Gly3Arg
ENST00000485991.5:n.1709G>C
NM_001145252.1:c.412G>C NP_001138724.1:p.Gly138Arg
NM_002621.2:c.412G>C , LRG_129t1:c.412G>C NP_002612.1:p.Gly138Arg
XM_017029575.1:c.7G>C XP_016885064.1:p.Gly3Arg
NM_001145252.3:c.412G>C MANE Select NP_001138724.1:p.Gly138Arg