Canonical Allele Identifier: CA1519927983

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186267196_186267197delinsGT , CM000666.2:g.186267196_186267197delinsGT	GRCh38
NC_000004.11:g.187188350_187188351delinsGT , CM000666.1:g.187188350_187188351delinsGT	GRCh37
NC_000004.10:g.187425344_187425345delinsGT	NCBI36
NG_008051.1:g.6233_6234delinsGT , LRG_583:g.6233_6234delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.55+5_55+6delinsGT MANE Select	ENSP00000384957.2:n.55+5_55+6delinsGT
ENST00000264692.8:c.55+5_55+6delinsGT	ENSP00000264692.5:n.55+5_55+6delinsGT
ENST00000403665.6:c.55+5_55+6delinsGT	ENSP00000384957.2:n.55+5_55+6delinsGT
ENST00000492972.6:c.55+5_55+6delinsGT	ENSP00000424479.1:n.55+5_55+6delinsGT
NM_000128.3:c.55+5_55+6delinsGT , LRG_583t1:c.55+5_55+6delinsGT	NP_000119.1:n.55+5_55+6delinsGT
XM_005262821.2:c.55+5_55+6delinsGT	XP_005262878.1:n.55+5_55+6delinsGT
XM_005262822.2:c.55+5_55+6delinsGT	XP_005262879.1:n.55+5_55+6delinsGT
XM_005262823.2:c.55+5_55+6delinsGT	XP_005262880.1:n.55+5_55+6delinsGT
XM_005262824.1:c.55+5_55+6delinsGT	XP_005262881.1:n.55+5_55+6delinsGT
XM_006714137.1:c.55+5_55+6delinsGT	XP_006714200.1:n.55+5_55+6delinsGT
XR_938706.1:n.407+5_407+6delinsGT
XR_938707.1:n.407+5_407+6delinsGT
NM_001354804.1:c.55+5_55+6delinsGT	NP_001341733.1:n.55+5_55+6delinsGT
XM_005262821.4:c.55+5_55+6delinsGT	XP_005262878.1:n.55+5_55+6delinsGT
XM_005262822.4:c.55+5_55+6delinsGT	XP_005262879.1:n.55+5_55+6delinsGT
XM_005262823.4:c.55+5_55+6delinsGT	XP_005262880.1:n.55+5_55+6delinsGT
XM_006714137.3:c.55+5_55+6delinsGT	XP_006714200.1:n.55+5_55+6delinsGT
XM_017007884.2:c.55+5_55+6delinsGT	XP_016863373.1:n.55+5_55+6delinsGT
XM_017007885.2:c.55+5_55+6delinsGT	XP_016863374.1:n.55+5_55+6delinsGT
XM_017007886.2:c.55+5_55+6delinsGT	XP_016863375.1:n.55+5_55+6delinsGT
XR_001741172.2:n.388+5_388+6delinsGT
NM_000128.4:c.55+5_55+6delinsGT MANE Select	NP_000119.1:n.55+5_55+6delinsGT
NM_001354804.2:c.55+5_55+6delinsGT	NP_001341733.1:n.55+5_55+6delinsGT