Canonical Allele Identifier: CA2672902494

Gene: F11

Linked Data

• gnomAD v4: 4-186280500-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186280503del , CM000666.2:g.186280503del	GRCh38
NC_000004.11:g.187201657del , CM000666.1:g.187201657del	GRCh37
NC_000004.10:g.187438651del	NCBI36
NG_008051.1:g.19540del , LRG_583:g.19540del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1058del MANE Select	ENSP00000384957.2:p.Asn353ThrfsTer19
ENST00000264692.8:c.896del	ENSP00000264692.5:p.Asn299ThrfsTer19
ENST00000403665.6:c.1058del	ENSP00000384957.2:p.Asn353ThrfsTer19
ENST00000452239.1:c.505del
NM_000128.3:c.1058del , LRG_583t1:c.1058del	NP_000119.1:p.Asn353ThrfsTer19
XM_005262821.2:c.1061del	XP_005262878.1:p.Asn354ThrfsTer19
XM_005262822.2:c.1061del	XP_005262879.1:p.Asn354ThrfsTer19
XM_005262823.2:c.791del	XP_005262880.1:p.Asn264ThrfsTer19
XM_005262824.1:c.1061del	XP_005262881.1:p.Asn354ThrfsTer19
XM_006714137.1:c.1013del	XP_006714200.1:p.Asn338ThrfsTer19
XR_938706.1:n.1413del
XR_938707.1:n.1413del
XM_005262821.4:c.1061del	XP_005262878.1:p.Asn354ThrfsTer19
XM_005262822.4:c.1061del	XP_005262879.1:p.Asn354ThrfsTer19
XM_005262823.4:c.791del	XP_005262880.1:p.Asn264ThrfsTer19
XM_006714137.3:c.1013del	XP_006714200.1:p.Asn338ThrfsTer19
XM_017007884.2:c.1061del	XP_016863373.1:p.Asn354ThrfsTer19
XM_017007885.2:c.1061del	XP_016863374.1:p.Asn354ThrfsTer19
XM_017007886.2:c.1058del	XP_016863375.1:p.Asn353ThrfsTer19
XR_001741172.2:n.1479del
NM_000128.4:c.1058del MANE Select	NP_000119.1:p.Asn353ThrfsTer19