Canonical Allele Identifier: CA112151620

Gene: F11

Linked Data

• dbSNP Id: rs35063152
• MyVariant Identifiers: chr4:g.187195885_187195886insC (hg19) ; chr4:g.186274731_186274732insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186274731_186274732insC , CM000666.2:g.186274731_186274732insC	GRCh38
NC_000004.11:g.187195885_187195886insC , CM000666.1:g.187195885_187195886insC	GRCh37
NC_000004.10:g.187432879_187432880insC	NCBI36
NG_008051.1:g.13768_13769insC , LRG_583:g.13768_13769insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.485+456_485+457insC MANE Select	ENSP00000384957.2:n.485+456_485+457insC
ENST00000264692.8:c.324-1056_324-1055insC	ENSP00000264692.5:n.324-1056_324-1055insC
ENST00000403665.6:c.485+456_485+457insC	ENSP00000384957.2:n.485+456_485+457insC
ENST00000492972.6:c.*452_*453insC	ENSP00000424479.1:n.*452_*453insC
NM_000128.3:c.485+456_485+457insC , LRG_583t1:c.485+456_485+457insC	NP_000119.1:n.485+456_485+457insC
XM_005262821.2:c.485+456_485+457insC	XP_005262878.1:n.485+456_485+457insC
XM_005262822.2:c.485+456_485+457insC	XP_005262879.1:n.485+456_485+457insC
XM_005262823.2:c.485+456_485+457insC	XP_005262880.1:n.485+456_485+457insC
XM_005262824.1:c.485+456_485+457insC	XP_005262881.1:n.485+456_485+457insC
XM_006714137.1:c.485+456_485+457insC	XP_006714200.1:n.485+456_485+457insC
XR_938706.1:n.837+456_837+457insC
XR_938707.1:n.837+456_837+457insC
NM_001354804.1:c.*452_*453insC	NP_001341733.1:n.*452_*453insC
XM_005262821.4:c.485+456_485+457insC	XP_005262878.1:n.485+456_485+457insC
XM_005262822.4:c.485+456_485+457insC	XP_005262879.1:n.485+456_485+457insC
XM_005262823.4:c.485+456_485+457insC	XP_005262880.1:n.485+456_485+457insC
XM_006714137.3:c.485+456_485+457insC	XP_006714200.1:n.485+456_485+457insC
XM_017007884.2:c.485+456_485+457insC	XP_016863373.1:n.485+456_485+457insC
XM_017007885.2:c.485+456_485+457insC	XP_016863374.1:n.485+456_485+457insC
XM_017007886.2:c.485+456_485+457insC	XP_016863375.1:n.485+456_485+457insC
XR_001741172.2:n.818+456_818+457insC
NM_000128.4:c.485+456_485+457insC MANE Select	NP_000119.1:n.485+456_485+457insC
NM_001354804.2:c.*452_*453insC	NP_001341733.1:n.*452_*453insC