Canonical Allele Identifier: CA412838878

Gene: CFP

Linked Data

• gnomAD v4: X-47627642-C-A
• MyVariant Identifiers: chrX:g.47487041C>A (hg19) ; chrX:g.47627642C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47627642C>A , CM000685.2:g.47627642C>A	GRCh38
NC_000023.10:g.47487041C>A , CM000685.1:g.47487041C>A	GRCh37
NC_000023.9:g.47371985C>A	NCBI36
NG_009893.1:g.7664G>T , LRG_129:g.7664G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396992.8:c.404-1G>T MANE Select	ENSP00000380189.3:n.404-1G>T
ENST00000640573.1:n.642-1G>T
ENST00000247153.7:c.404-1G>T	ENSP00000247153.3:n.404-1G>T
ENST00000377005.6:c.404-1G>T	ENSP00000366204.2:n.404-1G>T
ENST00000396992.7:c.404-1G>T	ENSP00000380189.3:n.404-1G>T
ENST00000469388.1:c.-2-1G>T	ENSP00000418258.1:n.-2-1G>T
ENST00000485991.5:n.1701-1G>T
NM_001145252.1:c.404-1G>T	NP_001138724.1:n.404-1G>T
NM_002621.2:c.404-1G>T , LRG_129t1:c.404-1G>T	NP_002612.1:n.404-1G>T
XM_017029575.1:c.-2-1G>T	XP_016885064.1:n.-2-1G>T
NM_001145252.3:c.404-1G>T MANE Select	NP_001138724.1:n.404-1G>T