Canonical Allele Identifier: CA10398960

Gene: CFP

Linked Data

• ClinVar Variation Id: 2995401
• ClinVar RCV Id: RCV003851008
• dbSNP Id: rs373347141
• ExAC: X:47487046 G / C
• gnomAD v2: X-47487046-G-C
• gnomAD v3: X-47627647-G-C
• gnomAD v4: X-47627647-G-C
• MyVariant Identifiers: chrX:g.47487046G>C (hg19) ; chrX:g.47627647G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47627647G>C , CM000685.2:g.47627647G>C	GRCh38
NC_000023.10:g.47487046G>C , CM000685.1:g.47487046G>C	GRCh37
NC_000023.9:g.47371990G>C	NCBI36
NG_009893.1:g.7659C>G , LRG_129:g.7659C>G

Transcript Alleles

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