Canonical Allele Identifier: CA1519935944

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186280189_186280190delinsAG , CM000666.2:g.186280189_186280190delinsAG	GRCh38
NC_000004.11:g.187201343_187201344delinsAG , CM000666.1:g.187201343_187201344delinsAG	GRCh37
NC_000004.10:g.187438337_187438338delinsAG	NCBI36
NG_008051.1:g.19226_19227delinsAG , LRG_583:g.19226_19227delinsAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.866-34_866-33delinsAG MANE Select	ENSP00000384957.2:n.866-34_866-33delinsAG...
ENST00000264692.8:c.704-34_704-33delinsAG	ENSP00000264692.5:n.704-34_704-33delinsAG...
ENST00000403665.6:c.866-34_866-33delinsAG	ENSP00000384957.2:n.866-34_866-33delinsAG...
ENST00000452239.1:c.313-34_313-33delinsAG
NM_000128.3:c.866-34_866-33delinsAG , LRG_583t1:c.866-34_866-33delinsAG	NP_000119.1:n.866-34_866-33delinsAG
XM_005262821.2:c.866-34_866-33delinsAG	XP_005262878.1:n.866-34_866-33delinsAG
XM_005262822.2:c.866-34_866-33delinsAG	XP_005262879.1:n.866-34_866-33delinsAG
XM_005262823.2:c.596-34_596-33delinsAG	XP_005262880.1:n.596-34_596-33delinsAG
XM_005262824.1:c.866-34_866-33delinsAG	XP_005262881.1:n.866-34_866-33delinsAG
XM_006714137.1:c.865+68_865+69delinsAG	XP_006714200.1:n.865+68_865+69delinsAG
XR_938706.1:n.1218-34_1218-33delinsAG
XR_938707.1:n.1218-34_1218-33delinsAG
XM_005262821.4:c.866-34_866-33delinsAG	XP_005262878.1:n.866-34_866-33delinsAG
XM_005262822.4:c.866-34_866-33delinsAG	XP_005262879.1:n.866-34_866-33delinsAG
XM_005262823.4:c.596-34_596-33delinsAG	XP_005262880.1:n.596-34_596-33delinsAG
XM_006714137.3:c.865+68_865+69delinsAG	XP_006714200.1:n.865+68_865+69delinsAG
XM_017007884.2:c.866-34_866-33delinsAG	XP_016863373.1:n.866-34_866-33delinsAG
XM_017007885.2:c.866-34_866-33delinsAG	XP_016863374.1:n.866-34_866-33delinsAG
XM_017007886.2:c.866-34_866-33delinsAG	XP_016863375.1:n.866-34_866-33delinsAG
XR_001741172.2:n.1199-34_1199-33delinsAG
NM_000128.4:c.866-34_866-33delinsAG MANE Select	NP_000119.1:n.866-34_866-33delinsAG