Canonical Allele Identifier: CA1519936142

Gene: F11

Linked Data

• dbSNP Id: rs1740727003
• gnomAD v4: 4-186280567-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186280571del , CM000666.2:g.186280571del	GRCh38
NC_000004.11:g.187201725del , CM000666.1:g.187201725del	GRCh37
NC_000004.10:g.187438719del	NCBI36
NG_008051.1:g.19608del , LRG_583:g.19608del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1126del MANE Select	ENSP00000384957.2:p.Met376TrpfsTer28
ENST00000264692.8:c.964del	ENSP00000264692.5:p.Met322TrpfsTer28
ENST00000403665.6:c.1126del	ENSP00000384957.2:p.Met376TrpfsTer28
ENST00000452239.1:c.573del
NM_000128.3:c.1126del , LRG_583t1:c.1126del	NP_000119.1:p.Met376TrpfsTer28
XM_005262821.2:c.1129del	XP_005262878.1:p.Met377TrpfsTer28
XM_005262822.2:c.1129del	XP_005262879.1:p.Met377TrpfsTer28
XM_005262823.2:c.859del	XP_005262880.1:p.Met287TrpfsTer28
XM_005262824.1:c.1129del	XP_005262881.1:p.Met377TrpfsTer28
XM_006714137.1:c.1081del	XP_006714200.1:p.Met361TrpfsTer28
XR_938706.1:n.1481del
XR_938707.1:n.1481del
XM_005262821.4:c.1129del	XP_005262878.1:p.Met377TrpfsTer28
XM_005262822.4:c.1129del	XP_005262879.1:p.Met377TrpfsTer28
XM_005262823.4:c.859del	XP_005262880.1:p.Met287TrpfsTer28
XM_006714137.3:c.1081del	XP_006714200.1:p.Met361TrpfsTer28
XM_017007884.2:c.1129del	XP_016863373.1:p.Met377TrpfsTer10
XM_017007885.2:c.1129del	XP_016863374.1:p.Met377TrpfsTer10
XM_017007886.2:c.1126del	XP_016863375.1:p.Met376TrpfsTer10
XR_001741172.2:n.1547del
NM_000128.4:c.1126del MANE Select	NP_000119.1:p.Met376TrpfsTer28