Canonical Allele Identifier: CA641493837

Gene: CFP

Linked Data

• dbSNP Id: rs1390809634
• gnomAD v2: X-47487236-GCA-G
• gnomAD v3: X-47627837-GCA-G
• gnomAD v4: X-47627837-GCA-G
• MyVariant Identifiers: chrX:g.47487237_47487238del (hg19) ; chrX:g.47627838_47627839del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47627840_47627841del , CM000685.2:g.47627840_47627841del	GRCh38
NC_000023.10:g.47487239_47487240del , CM000685.1:g.47487239_47487240del	GRCh37
NC_000023.9:g.47372183_47372184del	NCBI36
NG_009893.1:g.7467_7468del , LRG_129:g.7467_7468del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396992.8:c.404-198_404-197del MANE Select	ENSP00000380189.3:n.404-198_404-197del
ENST00000640573.1:n.642-198_642-197del
ENST00000247153.7:c.404-198_404-197del	ENSP00000247153.3:n.404-198_404-197del
ENST00000377005.6:c.404-198_404-197del	ENSP00000366204.2:n.404-198_404-197del
ENST00000396992.7:c.404-198_404-197del	ENSP00000380189.3:n.404-198_404-197del
ENST00000469388.1:c.-2-198_-2-197del	ENSP00000418258.1:n.-2-198_-2-197del
ENST00000485991.5:n.1701-198_1701-197del
NM_001145252.1:c.404-198_404-197del	NP_001138724.1:n.404-198_404-197del
NM_002621.2:c.404-198_404-197del , LRG_129t1:c.404-198_404-197del	NP_002612.1:n.404-198_404-197del
XM_017029575.1:c.-2-198_-2-197del	XP_016885064.1:n.-2-198_-2-197del
NM_001145252.3:c.404-198_404-197del MANE Select	NP_001138724.1:n.404-198_404-197del