Canonical Allele Identifier: CA2820776314

Gene: CFP

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47627766_47627767insAACAC , CM000685.2:g.47627766_47627767insAACAC	GRCh38
NC_000023.10:g.47487165_47487166insAACAC , CM000685.1:g.47487165_47487166insAACAC	GRCh37
NC_000023.9:g.47372109_47372110insAACAC	NCBI36
NG_009893.1:g.7539_7540insGTGTT , LRG_129:g.7539_7540insGTGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396992.8:c.404-126_404-125insGTGTT MANE Select	ENSP00000380189.3:n.404-126_404-125insGTGTT
ENST00000640573.1:n.642-126_642-125insGTGTT
ENST00000247153.7:c.404-126_404-125insGTGTT	ENSP00000247153.3:n.404-126_404-125insGTGTT
ENST00000377005.6:c.404-126_404-125insGTGTT	ENSP00000366204.2:n.404-126_404-125insGTGTT
ENST00000396992.7:c.404-126_404-125insGTGTT	ENSP00000380189.3:n.404-126_404-125insGTGTT
ENST00000469388.1:c.-2-126_-2-125insGTGTT	ENSP00000418258.1:n.-2-126_-2-125insGTGTT
ENST00000485991.5:n.1701-126_1701-125insGTGTT
NM_001145252.1:c.404-126_404-125insGTGTT	NP_001138724.1:n.404-126_404-125insGTGTT
NM_002621.2:c.404-126_404-125insGTGTT , LRG_129t1:c.404-126_404-125insGTGTT	NP_002612.1:n.404-126_404-125insGTGTT
XM_017029575.1:c.-2-126_-2-125insGTGTT	XP_016885064.1:n.-2-126_-2-125insGTGTT
NM_001145252.3:c.404-126_404-125insGTGTT MANE Select	NP_001138724.1:n.404-126_404-125insGTGTT