Canonical Allele Identifier: CA2427988901

Gene: CFP

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47627564G= , CM000685.2:g.47627564G=	GRCh38
NC_000023.10:g.47486963G= , CM000685.1:g.47486963G=	GRCh37
NC_000023.9:g.47371907G=	NCBI36
NG_009893.1:g.7742C= , LRG_129:g.7742C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396992.8:c.481C= MANE Select	ENSP00000380189.3:p.Arg161=
ENST00000640573.1:n.719C=
ENST00000247153.7:c.481C=	ENSP00000247153.3:p.Arg161=
ENST00000377005.6:c.481C=	ENSP00000366204.2:p.Arg161=
ENST00000396992.7:c.481C=	ENSP00000380189.3:p.Arg161=
ENST00000469388.1:c.76C=	ENSP00000418258.1:p.Arg26=
ENST00000485991.5:n.1778C=
NM_001145252.1:c.481C=	NP_001138724.1:p.Arg161=
NM_002621.2:c.481C= , LRG_129t1:c.481C=	NP_002612.1:p.Arg161=
XM_017029575.1:c.76C=	XP_016885064.1:p.Arg26=
NM_001145252.3:c.481C= MANE Select	NP_001138724.1:p.Arg161=