Canonical Allele Identifier: CA2672904186

Gene: F11 F11-AS1

Linked Data

• gnomAD v4: 4-186288608-AGTGT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186288610_186288613del , CM000666.2:g.186288610_186288613del	GRCh38
NC_000004.11:g.187209764_187209767del , CM000666.1:g.187209764_187209767del	GRCh37
NC_000004.10:g.187446758_187446761del	NCBI36
NG_008051.1:g.27647_27650del , LRG_583:g.27647_27650del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1874_1877del (F11) MANE Select	ENSP00000384957.2:p.Val625GlufsTer11
ENST00000264691.4:c.474_477del (F11)
ENST00000264692.8:c.1712_1715del (F11)	ENSP00000264692.5:p.Val571GlufsTer11
ENST00000403665.6:c.1874_1877del (F11)	ENSP00000384957.2:p.Val625GlufsTer11
ENST00000503841.1:n.393_396del (F11)
NM_000128.3:c.1874_1877del , LRG_583t1:c.1874_1877del (F11)	NP_000119.1:p.Val625GlufsTer11
NR_033900.1:n.882_885del (F11-AS1)
XM_005262821.2:c.1877_1880del (F11)	XP_005262878.1:p.Val626GlufsTer11
XM_005262822.2:c.1781_1784del (F11)	XP_005262879.1:p.Val594GlufsTer11
XM_005262823.2:c.1607_1610del (F11)	XP_005262880.1:p.Val536GlufsTer11
XM_006714137.1:c.1829_1832del (F11)	XP_006714200.1:p.Val610GlufsTer11
XM_005262821.4:c.1877_1880del (F11)	XP_005262878.1:p.Val626GlufsTer11
XM_005262822.4:c.1781_1784del (F11)	XP_005262879.1:p.Val594GlufsTer11
XM_005262823.4:c.1607_1610del (F11)	XP_005262880.1:p.Val536GlufsTer11
XM_006714137.3:c.1829_1832del (F11)	XP_006714200.1:p.Val610GlufsTer11
NM_000128.4:c.1874_1877del (F11) MANE Select	NP_000119.1:p.Val625GlufsTer11