Canonical Allele Identifier: CA2427988917

Gene: CFP

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396992.8:c.412G= MANE Select	ENSP00000380189.3:p.Gly138=
ENST00000640573.1:n.650G=
ENST00000247153.7:c.412G=	ENSP00000247153.3:p.Gly138=
ENST00000377005.6:c.412G=	ENSP00000366204.2:p.Gly138=
ENST00000396992.7:c.412G=	ENSP00000380189.3:p.Gly138=
ENST00000469388.1:c.7G=	ENSP00000418258.1:p.Gly3=
ENST00000485991.5:n.1709G=
NM_001145252.1:c.412G=	NP_001138724.1:p.Gly138=
NM_002621.2:c.412G= , LRG_129t1:c.412G=	NP_002612.1:p.Gly138=
XM_017029575.1:c.7G=	XP_016885064.1:p.Gly3=
NM_001145252.3:c.412G= MANE Select	NP_001138724.1:p.Gly138=