Canonical Allele Identifier: CA2427988996

Gene: CFP

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47627837_47627839delinsGCA , CM000685.2:g.47627837_47627839delinsGCA	GRCh38
NC_000023.10:g.47487236_47487238delinsGCA , CM000685.1:g.47487236_47487238delinsGCA	GRCh37
NC_000023.9:g.47372180_47372182delinsGCA	NCBI36
NG_009893.1:g.7467_7469delinsTGC , LRG_129:g.7467_7469delinsTGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396992.8:c.404-198_404-196delinsTGC MANE Select	ENSP00000380189.3:n.404-198_404-196delinsTGC
ENST00000640573.1:n.642-198_642-196delinsTGC
ENST00000247153.7:c.404-198_404-196delinsTGC	ENSP00000247153.3:n.404-198_404-196delinsTGC
ENST00000377005.6:c.404-198_404-196delinsTGC	ENSP00000366204.2:n.404-198_404-196delinsTGC
ENST00000396992.7:c.404-198_404-196delinsTGC	ENSP00000380189.3:n.404-198_404-196delinsTGC
ENST00000469388.1:c.-2-198_-2-196delinsTGC	ENSP00000418258.1:n.-2-198_-2-196delinsTGC
ENST00000485991.5:n.1701-198_1701-196delinsTGC
NM_001145252.1:c.404-198_404-196delinsTGC	NP_001138724.1:n.404-198_404-196delinsTGC
NM_002621.2:c.404-198_404-196delinsTGC , LRG_129t1:c.404-198_404-196delinsTGC	NP_002612.1:n.404-198_404-196delinsTGC
XM_017029575.1:c.-2-198_-2-196delinsTGC	XP_016885064.1:n.-2-198_-2-196delinsTGC
NM_001145252.3:c.404-198_404-196delinsTGC MANE Select	NP_001138724.1:n.404-198_404-196delinsTGC