Canonical Allele Identifier: CA2427988952

Gene: CFP

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47627756T= , CM000685.2:g.47627756T=	GRCh38
NC_000023.10:g.47487155T= , CM000685.1:g.47487155T=	GRCh37
NC_000023.9:g.47372099T=	NCBI36
NG_009893.1:g.7550A= , LRG_129:g.7550A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396992.8:c.404-115A= MANE Select	ENSP00000380189.3:n.404-115A=
ENST00000640573.1:n.642-115A=
ENST00000247153.7:c.404-115A=	ENSP00000247153.3:n.404-115A=
ENST00000377005.6:c.404-115A=	ENSP00000366204.2:n.404-115A=
ENST00000396992.7:c.404-115A=	ENSP00000380189.3:n.404-115A=
ENST00000469388.1:c.-2-115A=	ENSP00000418258.1:n.-2-115A=
ENST00000485991.5:n.1701-115A=
NM_001145252.1:c.404-115A=	NP_001138724.1:n.404-115A=
NM_002621.2:c.404-115A= , LRG_129t1:c.404-115A=	NP_002612.1:n.404-115A=
XM_017029575.1:c.-2-115A=	XP_016885064.1:n.-2-115A=
NM_001145252.3:c.404-115A= MANE Select	NP_001138724.1:n.404-115A=