Canonical Allele Identifier: CA792311635

Gene: F11

Linked Data

• dbSNP Id: rs1326590304
• gnomAD v4: 4-186280274-TG-T
• MyVariant Identifiers: chr4:g.187201429del (hg19) ; chr4:g.186280275del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186280276del , CM000666.2:g.186280276del	GRCh38
NC_000004.11:g.187201430del , CM000666.1:g.187201430del	GRCh37
NC_000004.10:g.187438424del	NCBI36
NG_008051.1:g.19313del , LRG_583:g.19313del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.919del MANE Select	ENSP00000384957.2:p.Asp307IlefsTer?
ENST00000264692.8:c.757del	ENSP00000264692.5:p.Asp253IlefsTer?
ENST00000403665.6:c.919del	ENSP00000384957.2:p.Asp307IlefsTer?
ENST00000452239.1:c.366del
NM_000128.3:c.919del , LRG_583t1:c.919del	NP_000119.1:p.Asp307IlefsTer?
XM_005262821.2:c.919del	XP_005262878.1:p.Asp307IlefsTer?
XM_005262822.2:c.919del	XP_005262879.1:p.Asp307IlefsTer?
XM_005262823.2:c.649del	XP_005262880.1:p.Asp217IlefsTer?
XM_005262824.1:c.919del	XP_005262881.1:p.Asp307IlefsTer?
XM_006714137.1:c.871del	XP_006714200.1:p.Asp291IlefsTer?
XR_938706.1:n.1271del
XR_938707.1:n.1271del
XM_005262821.4:c.919del	XP_005262878.1:p.Asp307IlefsTer?
XM_005262822.4:c.919del	XP_005262879.1:p.Asp307IlefsTer?
XM_005262823.4:c.649del	XP_005262880.1:p.Asp217IlefsTer?
XM_006714137.3:c.871del	XP_006714200.1:p.Asp291IlefsTer?
XM_017007884.2:c.919del	XP_016863373.1:p.Asp307IlefsTer?
XM_017007885.2:c.919del	XP_016863374.1:p.Asp307IlefsTer?
XM_017007886.2:c.919del	XP_016863375.1:p.Asp307IlefsTer?
XR_001741172.2:n.1252del
NM_000128.4:c.919del MANE Select	NP_000119.1:p.Asp307IlefsTer?