Canonical Allele Identifier: CA412838766

Gene: CFP

Linked Data

• MyVariant Identifiers: chrX:g.47486992G>T (hg19) ; chrX:g.47627593G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47627593G>T , CM000685.2:g.47627593G>T	GRCh38
NC_000023.10:g.47486992G>T , CM000685.1:g.47486992G>T	GRCh37
NC_000023.9:g.47371936G>T	NCBI36
NG_009893.1:g.7713C>A , LRG_129:g.7713C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396992.8:c.452C>A MANE Select	ENSP00000380189.3:p.Thr151Asn
ENST00000640573.1:n.690C>A
ENST00000247153.7:c.452C>A	ENSP00000247153.3:p.Thr151Asn
ENST00000377005.6:c.452C>A	ENSP00000366204.2:p.Thr151Asn
ENST00000396992.7:c.452C>A	ENSP00000380189.3:p.Thr151Asn
ENST00000469388.1:c.47C>A	ENSP00000418258.1:p.Thr16Asn
ENST00000485991.5:n.1749C>A
NM_001145252.1:c.452C>A	NP_001138724.1:p.Thr151Asn
NM_002621.2:c.452C>A , LRG_129t1:c.452C>A	NP_002612.1:p.Thr151Asn
XM_017029575.1:c.47C>A	XP_016885064.1:p.Thr16Asn
NM_001145252.3:c.452C>A MANE Select	NP_001138724.1:p.Thr151Asn