Canonical Allele Identifier: CA2427988902

Gene: CFP

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47627568G= , CM000685.2:g.47627568G=	GRCh38
NC_000023.10:g.47486967G= , CM000685.1:g.47486967G=	GRCh37
NC_000023.9:g.47371911G=	NCBI36
NG_009893.1:g.7738C= , LRG_129:g.7738C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000396992.8:c.477C= MANE Select	ENSP00000380189.3:p.Arg159=
ENST00000640573.1:n.715C=
ENST00000247153.7:c.477C=	ENSP00000247153.3:p.Arg159=
ENST00000377005.6:c.477C=	ENSP00000366204.2:p.Arg159=
ENST00000396992.7:c.477C=	ENSP00000380189.3:p.Arg159=
ENST00000469388.1:c.72C=	ENSP00000418258.1:p.Arg24=
ENST00000485991.5:n.1774C=
NM_001145252.1:c.477C=	NP_001138724.1:p.Arg159=
NM_002621.2:c.477C= , LRG_129t1:c.477C=	NP_002612.1:p.Arg159=
XM_017029575.1:c.72C=	XP_016885064.1:p.Arg24=
NM_001145252.3:c.477C= MANE Select	NP_001138724.1:p.Arg159=