Canonical Allele Identifier: CA1519927818

Gene: F11

Linked Data

• dbSNP Id: rs1739552050

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186266990_186266991insG , CM000666.2:g.186266990_186266991insG	GRCh38
NC_000004.11:g.187188144_187188145insG , CM000666.1:g.187188144_187188145insG	GRCh37
NC_000004.10:g.187425138_187425139insG	NCBI36
NG_008051.1:g.6027_6028insG , LRG_583:g.6027_6028insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.-1-146_-1-145insG MANE Select	ENSP00000384957.2:n.-1-146_-1-145insG
ENST00000264692.8:c.-1-146_-1-145insG	ENSP00000264692.5:n.-1-146_-1-145insG
ENST00000403665.6:c.-1-146_-1-145insG	ENSP00000384957.2:n.-1-146_-1-145insG
ENST00000492972.6:c.-1-146_-1-145insG	ENSP00000424479.1:n.-1-146_-1-145insG
NM_000128.3:c.-1-146_-1-145insG , LRG_583t1:c.-1-146_-1-145insG	NP_000119.1:n.-1-146_-1-145insG
XM_005262821.2:c.-1-146_-1-145insG	XP_005262878.1:n.-1-146_-1-145insG
XM_005262822.2:c.-1-146_-1-145insG	XP_005262879.1:n.-1-146_-1-145insG
XM_005262823.2:c.-1-146_-1-145insG	XP_005262880.1:n.-1-146_-1-145insG
XM_005262824.1:c.-1-146_-1-145insG	XP_005262881.1:n.-1-146_-1-145insG
XM_006714137.1:c.-1-146_-1-145insG	XP_006714200.1:n.-1-146_-1-145insG
XR_938706.1:n.352-146_352-145insG
XR_938707.1:n.352-146_352-145insG
NM_001354804.1:c.-1-146_-1-145insG	NP_001341733.1:n.-1-146_-1-145insG
XM_005262821.4:c.-1-146_-1-145insG	XP_005262878.1:n.-1-146_-1-145insG
XM_005262822.4:c.-1-146_-1-145insG	XP_005262879.1:n.-1-146_-1-145insG
XM_005262823.4:c.-1-146_-1-145insG	XP_005262880.1:n.-1-146_-1-145insG
XM_006714137.3:c.-1-146_-1-145insG	XP_006714200.1:n.-1-146_-1-145insG
XM_017007884.2:c.-1-146_-1-145insG	XP_016863373.1:n.-1-146_-1-145insG
XM_017007885.2:c.-1-146_-1-145insG	XP_016863374.1:n.-1-146_-1-145insG
XM_017007886.2:c.-1-146_-1-145insG	XP_016863375.1:n.-1-146_-1-145insG
XR_001741172.2:n.333-146_333-145insG
NM_000128.4:c.-1-146_-1-145insG MANE Select	NP_000119.1:n.-1-146_-1-145insG
NM_001354804.2:c.-1-146_-1-145insG	NP_001341733.1:n.-1-146_-1-145insG