Canonical Allele Identifier: CA516354361

Gene: CFP

Linked Data

• MyVariant Identifiers: chrX:g.47487006C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47627607C>T , CM000685.2:g.47627607C>T	GRCh38
NC_000023.10:g.47487006C>T , CM000685.1:g.47487006C>T	GRCh37
NC_000023.9:g.47371950C>T	NCBI36
NG_009893.1:g.7699G>A , LRG_129:g.7699G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396992.8:c.438G>A MANE Select	ENSP00000380189.3:p.Glu146=
ENST00000640573.1:n.676G>A
ENST00000247153.7:c.438G>A	ENSP00000247153.3:p.Glu146=
ENST00000377005.6:c.438G>A	ENSP00000366204.2:p.Glu146=
ENST00000396992.7:c.438G>A	ENSP00000380189.3:p.Glu146=
ENST00000469388.1:c.33G>A	ENSP00000418258.1:p.Glu11=
ENST00000485991.5:n.1735G>A
NM_001145252.1:c.438G>A	NP_001138724.1:p.Glu146=
NM_002621.2:c.438G>A , LRG_129t1:c.438G>A	NP_002612.1:p.Glu146=
XM_017029575.1:c.33G>A	XP_016885064.1:p.Glu11=
NM_001145252.3:c.438G>A MANE Select	NP_001138724.1:p.Glu146=