Canonical Allele Identifier: CA913103788

Gene: F11

Linked Data

• MyVariant Identifiers: chr4:g.187201495_187201496del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186280341_186280342del , CM000666.2:g.186280341_186280342del	GRCh38
NC_000004.11:g.187201495_187201496del , CM000666.1:g.187201495_187201496del	GRCh37
NC_000004.10:g.187438489_187438490del	NCBI36
NG_008051.1:g.19378_19379del , LRG_583:g.19378_19379del

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.984_985del MANE Select	ENSP00000384957.2:p.Gln328HisfsTer30
ENST00000264692.8:c.822_823del	ENSP00000264692.5:p.Gln274HisfsTer30
ENST00000403665.6:c.984_985del	ENSP00000384957.2:p.Gln328HisfsTer30
ENST00000452239.1:c.431_432del
NM_000128.3:c.984_985del , LRG_583t1:c.984_985del	NP_000119.1:p.Gln328HisfsTer30
XM_005262821.2:c.984_985del	XP_005262878.1:p.Gln328HisfsTer?
XM_005262822.2:c.984_985del	XP_005262879.1:p.Gln328HisfsTer?
XM_005262823.2:c.714_715del	XP_005262880.1:p.Gln238HisfsTer?
XM_005262824.1:c.984_985del	XP_005262881.1:p.Gln328HisfsTer?
XM_006714137.1:c.936_937del	XP_006714200.1:p.Gln312HisfsTer?
XR_938706.1:n.1336_1337del
XR_938707.1:n.1336_1337del
XM_005262821.4:c.984_985del	XP_005262878.1:p.Gln328HisfsTer?
XM_005262822.4:c.984_985del	XP_005262879.1:p.Gln328HisfsTer?
XM_005262823.4:c.714_715del	XP_005262880.1:p.Gln238HisfsTer?
XM_006714137.3:c.936_937del	XP_006714200.1:p.Gln312HisfsTer?
XM_017007884.2:c.984_985del	XP_016863373.1:p.Gln328HisfsTer?
XM_017007885.2:c.984_985del	XP_016863374.1:p.Gln328HisfsTer?
XM_017007886.2:c.984_985del	XP_016863375.1:p.Gln328HisfsTer30
XR_001741172.2:n.1317_1318del
NM_000128.4:c.984_985del MANE Select	NP_000119.1:p.Gln328HisfsTer30