Canonical Allele Identifier: CA2820776327

Gene: CFP

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47627841_47627863dup , CM000685.2:g.47627841_47627863dup	GRCh38
NC_000023.10:g.47487240_47487262dup , CM000685.1:g.47487240_47487262dup	GRCh37
NC_000023.9:g.47372184_47372206dup	NCBI36
NG_009893.1:g.7443_7465dup , LRG_129:g.7443_7465dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396992.8:c.404-222_404-200dup MANE Select	ENSP00000380189.3:n.404-222_404-200dup
ENST00000640573.1:n.642-222_642-200dup
ENST00000247153.7:c.404-222_404-200dup	ENSP00000247153.3:n.404-222_404-200dup
ENST00000377005.6:c.404-222_404-200dup	ENSP00000366204.2:n.404-222_404-200dup
ENST00000396992.7:c.404-222_404-200dup	ENSP00000380189.3:n.404-222_404-200dup
ENST00000469388.1:c.-2-222_-2-200dup	ENSP00000418258.1:n.-2-222_-2-200dup
ENST00000485991.5:n.1701-222_1701-200dup
NM_001145252.1:c.404-222_404-200dup	NP_001138724.1:n.404-222_404-200dup
NM_002621.2:c.404-222_404-200dup , LRG_129t1:c.404-222_404-200dup	NP_002612.1:n.404-222_404-200dup
XM_017029575.1:c.-2-222_-2-200dup	XP_016885064.1:n.-2-222_-2-200dup
NM_001145252.3:c.404-222_404-200dup MANE Select	NP_001138724.1:n.404-222_404-200dup