Canonical Allele Identifier: CA1519935998

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186280315_186280317delinsCTG , CM000666.2:g.186280315_186280317delinsCTG	GRCh38
NC_000004.11:g.187201469_187201471delinsCTG , CM000666.1:g.187201469_187201471delinsCTG	GRCh37
NC_000004.10:g.187438463_187438465delinsCTG	NCBI36
NG_008051.1:g.19352_19354delinsCTG , LRG_583:g.19352_19354delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.958_960delinsCTG MANE Select	ENSP00000384957.2:p.Leu320=
ENST00000264692.8:c.796_798delinsCTG	ENSP00000264692.5:p.Leu266=
ENST00000403665.6:c.958_960delinsCTG	ENSP00000384957.2:p.Leu320=
ENST00000452239.1:c.405_407delinsCTG
NM_000128.3:c.958_960delinsCTG , LRG_583t1:c.958_960delinsCTG	NP_000119.1:p.Leu320=
XM_005262821.2:c.958_960delinsCTG	XP_005262878.1:p.Leu320=
XM_005262822.2:c.958_960delinsCTG	XP_005262879.1:p.Leu320=
XM_005262823.2:c.688_690delinsCTG	XP_005262880.1:p.Leu230=
XM_005262824.1:c.958_960delinsCTG	XP_005262881.1:p.Leu320=
XM_006714137.1:c.910_912delinsCTG	XP_006714200.1:p.Leu304=
XR_938706.1:n.1310_1312delinsCTG
XR_938707.1:n.1310_1312delinsCTG
XM_005262821.4:c.958_960delinsCTG	XP_005262878.1:p.Leu320=
XM_005262822.4:c.958_960delinsCTG	XP_005262879.1:p.Leu320=
XM_005262823.4:c.688_690delinsCTG	XP_005262880.1:p.Leu230=
XM_006714137.3:c.910_912delinsCTG	XP_006714200.1:p.Leu304=
XM_017007884.2:c.958_960delinsCTG	XP_016863373.1:p.Leu320=
XM_017007885.2:c.958_960delinsCTG	XP_016863374.1:p.Leu320=
XM_017007886.2:c.958_960delinsCTG	XP_016863375.1:p.Leu320=
XR_001741172.2:n.1291_1293delinsCTG
NM_000128.4:c.958_960delinsCTG MANE Select	NP_000119.1:p.Leu320=