Canonical Allele Identifier: CA2672902446

Gene: F11

Linked Data

• gnomAD v4: 4-186280094-C-CTTTG

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186280095_186280096insTTGT , CM000666.2:g.186280095_186280096insTTGT	GRCh38
NC_000004.11:g.187201249_187201250insTTGT , CM000666.1:g.187201249_187201250insTTGT	GRCh37
NC_000004.10:g.187438243_187438244insTTGT	NCBI36
NG_008051.1:g.19132_19133insTTGT , LRG_583:g.19132_19133insTTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.839_840insTTGT MANE Select	ENSP00000384957.2:p.Gln281CysfsTer19
ENST00000264692.8:c.677_678insTTGT	ENSP00000264692.5:p.Gln227CysfsTer19
ENST00000403665.6:c.839_840insTTGT	ENSP00000384957.2:p.Gln281CysfsTer19
ENST00000452239.1:c.286_287insTTGT
NM_000128.3:c.839_840insTTGT , LRG_583t1:c.839_840insTTGT	NP_000119.1:p.Gln281CysfsTer19
XM_005262821.2:c.839_840insTTGT	XP_005262878.1:p.Gln281CysfsTer19
XM_005262822.2:c.839_840insTTGT	XP_005262879.1:p.Gln281CysfsTer19
XM_005262823.2:c.569_570insTTGT	XP_005262880.1:p.Gln191CysfsTer19
XM_005262824.1:c.839_840insTTGT	XP_005262881.1:p.Gln281CysfsTer19
XM_006714137.1:c.839_840insTTGT	XP_006714200.1:p.Gln281CysfsTer?
XR_938706.1:n.1191_1192insTTGT
XR_938707.1:n.1191_1192insTTGT
XM_005262821.4:c.839_840insTTGT	XP_005262878.1:p.Gln281CysfsTer19
XM_005262822.4:c.839_840insTTGT	XP_005262879.1:p.Gln281CysfsTer19
XM_005262823.4:c.569_570insTTGT	XP_005262880.1:p.Gln191CysfsTer19
XM_006714137.3:c.839_840insTTGT	XP_006714200.1:p.Gln281CysfsTer?
XM_017007884.2:c.839_840insTTGT	XP_016863373.1:p.Gln281CysfsTer19
XM_017007885.2:c.839_840insTTGT	XP_016863374.1:p.Gln281CysfsTer19
XM_017007886.2:c.839_840insTTGT	XP_016863375.1:p.Gln281CysfsTer19
XR_001741172.2:n.1172_1173insTTGT
NM_000128.4:c.839_840insTTGT MANE Select	NP_000119.1:p.Gln281CysfsTer19