Canonical Allele Identifier: CA1519931348

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186271149_186271151delinsATG , CM000666.2:g.186271149_186271151delinsATG	GRCh38
NC_000004.11:g.187192303_187192305delinsATG , CM000666.1:g.187192303_187192305delinsATG	GRCh37
NC_000004.10:g.187429297_187429299delinsATG	NCBI36
NG_008051.1:g.10186_10188delinsATG , LRG_583:g.10186_10188delinsATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.56-460_56-458delinsATG MANE Select	ENSP00000384957.2:n.56-460_56-458delinsATG
ENST00000264692.8:c.56-460_56-458delinsATG	ENSP00000264692.5:n.56-460_56-458delinsATG
ENST00000403665.6:c.56-460_56-458delinsATG	ENSP00000384957.2:n.56-460_56-458delinsATG
ENST00000492972.6:c.56-460_56-458delinsATG	ENSP00000424479.1:n.56-460_56-458delinsATG
NM_000128.3:c.56-460_56-458delinsATG , LRG_583t1:c.56-460_56-458delinsATG	NP_000119.1:n.56-460_56-458delinsATG
XM_005262821.2:c.56-460_56-458delinsATG	XP_005262878.1:n.56-460_56-458delinsATG
XM_005262822.2:c.56-460_56-458delinsATG	XP_005262879.1:n.56-460_56-458delinsATG
XM_005262823.2:c.56-460_56-458delinsATG	XP_005262880.1:n.56-460_56-458delinsATG
XM_005262824.1:c.56-460_56-458delinsATG	XP_005262881.1:n.56-460_56-458delinsATG
XM_006714137.1:c.56-460_56-458delinsATG	XP_006714200.1:n.56-460_56-458delinsATG
XR_938706.1:n.408-460_408-458delinsATG
XR_938707.1:n.408-460_408-458delinsATG
NM_001354804.1:c.56-460_56-458delinsATG	NP_001341733.1:n.56-460_56-458delinsATG
XM_005262821.4:c.56-460_56-458delinsATG	XP_005262878.1:n.56-460_56-458delinsATG
XM_005262822.4:c.56-460_56-458delinsATG	XP_005262879.1:n.56-460_56-458delinsATG
XM_005262823.4:c.56-460_56-458delinsATG	XP_005262880.1:n.56-460_56-458delinsATG
XM_006714137.3:c.56-460_56-458delinsATG	XP_006714200.1:n.56-460_56-458delinsATG
XM_017007884.2:c.56-460_56-458delinsATG	XP_016863373.1:n.56-460_56-458delinsATG
XM_017007885.2:c.56-460_56-458delinsATG	XP_016863374.1:n.56-460_56-458delinsATG
XM_017007886.2:c.56-460_56-458delinsATG	XP_016863375.1:n.56-460_56-458delinsATG
XR_001741172.2:n.389-460_389-458delinsATG
NM_000128.4:c.56-460_56-458delinsATG MANE Select	NP_000119.1:n.56-460_56-458delinsATG
NM_001354804.2:c.56-460_56-458delinsATG	NP_001341733.1:n.56-460_56-458delinsATG