Canonical Allele Identifier: CA1519938508

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186285692_186285706delinsAATAAAAGAGGACAC , CM000666.2:g.186285692_186285706delinsAATAAAAGAGGACAC	GRCh38
NC_000004.11:g.187206846_187206860delinsAATAAAAGAGGACAC , CM000666.1:g.187206846_187206860delinsAATAAAAGAGGACAC	GRCh37
NC_000004.10:g.187443840_187443854delinsAATAAAAGAGGACAC	NCBI36
NG_008051.1:g.24729_24743delinsAATAAAAGAGGACAC , LRG_583:g.24729_24743delinsAATAAAAGAGGACAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1359_1373delinsAATAAAAGAGGACAC MANE Select	ENSP00000384957.2:p.Glu453=
ENST00000264691.4:c.55_69delinsAATAAAAGAGGACAC
ENST00000264692.8:c.1197_1211delinsAATAAAAGAGGACAC	ENSP00000264692.5:p.Glu399=
ENST00000403665.6:c.1359_1373delinsAATAAAAGAGGACAC	ENSP00000384957.2:p.Glu453=
NM_000128.3:c.1359_1373delinsAATAAAAGAGGACAC , LRG_583t1:c.1359_1373delinsAATAAAAGAGGACAC	NP_000119.1:p.Glu453=
XM_005262821.2:c.1362_1376delinsAATAAAAGAGGACAC	XP_005262878.1:p.Glu454=
XM_005262822.2:c.1362_1376delinsAATAAAAGAGGACAC	XP_005262879.1:p.Glu454=
XM_005262823.2:c.1092_1106delinsAATAAAAGAGGACAC	XP_005262880.1:p.Glu364=
XM_005262824.1:c.1362_1376delinsAATAAAAGAGGACAC	XP_005262881.1:p.Glu454=
XM_006714137.1:c.1314_1328delinsAATAAAAGAGGACAC	XP_006714200.1:p.Glu438=
XR_938706.1:n.1767_1781delinsAATAAAAGAGGACAC
XR_938707.1:n.1767_1781delinsAATAAAAGAGGACAC
XM_005262821.4:c.1362_1376delinsAATAAAAGAGGACAC	XP_005262878.1:p.Glu454=
XM_005262822.4:c.1362_1376delinsAATAAAAGAGGACAC	XP_005262879.1:p.Glu454=
XM_005262823.4:c.1092_1106delinsAATAAAAGAGGACAC	XP_005262880.1:p.Glu364=
XM_006714137.3:c.1314_1328delinsAATAAAAGAGGACAC	XP_006714200.1:p.Glu438=
XR_001741172.2:n.1833_1847delinsAATAAAAGAGGACAC
NM_000128.4:c.1359_1373delinsAATAAAAGAGGACAC MANE Select	NP_000119.1:p.Glu453=