Canonical Allele Identifier: CA2672902480

Gene: F11

Linked Data

• gnomAD v4: 4-186284153-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284155del , CM000666.2:g.186284155del	GRCh38
NC_000004.11:g.187205309del , CM000666.1:g.187205309del	GRCh37
NC_000004.10:g.187442303del	NCBI36
NG_008051.1:g.23192del , LRG_583:g.23192del

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1199del MANE Select	ENSP00000384957.2:p.Pro400ArgfsTer4
ENST00000264692.8:c.1037del	ENSP00000264692.5:p.Pro346ArgfsTer4
ENST00000403665.6:c.1199del	ENSP00000384957.2:p.Pro400ArgfsTer4
NM_000128.3:c.1199del , LRG_583t1:c.1199del	NP_000119.1:p.Pro400ArgfsTer4
XM_005262821.2:c.1202del	XP_005262878.1:p.Pro401ArgfsTer4
XM_005262822.2:c.1202del	XP_005262879.1:p.Pro401ArgfsTer4
XM_005262823.2:c.932del	XP_005262880.1:p.Pro311ArgfsTer4
XM_005262824.1:c.1202del	XP_005262881.1:p.Pro401ArgfsTer4
XM_006714137.1:c.1154del	XP_006714200.1:p.Pro385ArgfsTer4
XR_938706.1:n.1607del
XR_938707.1:n.1607del
XM_005262821.4:c.1202del	XP_005262878.1:p.Pro401ArgfsTer4
XM_005262822.4:c.1202del	XP_005262879.1:p.Pro401ArgfsTer4
XM_005262823.4:c.932del	XP_005262880.1:p.Pro311ArgfsTer4
XM_006714137.3:c.1154del	XP_006714200.1:p.Pro385ArgfsTer4
XM_017007884.2:c.*2171del	XP_016863373.1:n.*2171del
XM_017007885.2:c.*67del	XP_016863374.1:n.*67del
XR_001741172.2:n.1673del
NM_000128.4:c.1199del MANE Select	NP_000119.1:p.Pro400ArgfsTer4