Canonical Allele Identifier: CA2672902442

Gene: F11

Linked Data

• gnomAD v4: 4-186280036-TGA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186280040_186280041del , CM000666.2:g.186280040_186280041del	GRCh38
NC_000004.11:g.187201194_187201195del , CM000666.1:g.187201194_187201195del	GRCh37
NC_000004.10:g.187438188_187438189del	NCBI36
NG_008051.1:g.19077_19078del , LRG_583:g.19077_19078del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.784_785del MANE Select	ENSP00000384957.2:p.Ser262TrpfsTer8
ENST00000264692.8:c.622_623del	ENSP00000264692.5:p.Ser208TrpfsTer8
ENST00000403665.6:c.784_785del	ENSP00000384957.2:p.Ser262TrpfsTer8
ENST00000452239.1:c.231_232del
NM_000128.3:c.784_785del , LRG_583t1:c.784_785del	NP_000119.1:p.Ser262TrpfsTer8
XM_005262821.2:c.784_785del	XP_005262878.1:p.Ser262TrpfsTer8
XM_005262822.2:c.784_785del	XP_005262879.1:p.Ser262TrpfsTer8
XM_005262823.2:c.514_515del	XP_005262880.1:p.Ser172TrpfsTer8
XM_005262824.1:c.784_785del	XP_005262881.1:p.Ser262TrpfsTer8
XM_006714137.1:c.784_785del	XP_006714200.1:p.Ser262TrpfsTer8
XR_938706.1:n.1136_1137del
XR_938707.1:n.1136_1137del
XM_005262821.4:c.784_785del	XP_005262878.1:p.Ser262TrpfsTer8
XM_005262822.4:c.784_785del	XP_005262879.1:p.Ser262TrpfsTer8
XM_005262823.4:c.514_515del	XP_005262880.1:p.Ser172TrpfsTer8
XM_006714137.3:c.784_785del	XP_006714200.1:p.Ser262TrpfsTer8
XM_017007884.2:c.784_785del	XP_016863373.1:p.Ser262TrpfsTer8
XM_017007885.2:c.784_785del	XP_016863374.1:p.Ser262TrpfsTer8
XM_017007886.2:c.784_785del	XP_016863375.1:p.Ser262TrpfsTer8
XR_001741172.2:n.1117_1118del
NM_000128.4:c.784_785del MANE Select	NP_000119.1:p.Ser262TrpfsTer8