Canonical Allele Identifier: CA1519938545
Gene: F11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186285784T= , CM000666.2:g.186285784T= GRCh38
NC_000004.11:g.187206938T= , CM000666.1:g.187206938T= GRCh37
NC_000004.10:g.187443932T= NCBI36
NG_008051.1:g.24821T= , LRG_583:g.24821T=

Transcript Alleles

HGVS Amino-acid change
ENST00000403665.7:c.1451T= MANE Select ENSP00000384957.2:p.Leu484=
ENST00000264691.4:c.147T=
ENST00000264692.8:c.1289T= ENSP00000264692.5:p.Leu430=
ENST00000403665.6:c.1451T= ENSP00000384957.2:p.Leu484=
NM_000128.3:c.1451T= , LRG_583t1:c.1451T= NP_000119.1:p.Leu484=
XM_005262821.2:c.1454T= XP_005262878.1:p.Leu485=
XM_005262822.2:c.1454T= XP_005262879.1:p.Leu485=
XM_005262823.2:c.1184T= XP_005262880.1:p.Leu395=
XM_005262824.1:c.1454T= XP_005262881.1:p.Leu485=
XM_006714137.1:c.1406T= XP_006714200.1:p.Leu469=
XR_938706.1:n.1859T=
XR_938707.1:n.1859T=
XM_005262821.4:c.1454T= XP_005262878.1:p.Leu485=
XM_005262822.4:c.1454T= XP_005262879.1:p.Leu485=
XM_005262823.4:c.1184T= XP_005262880.1:p.Leu395=
XM_006714137.3:c.1406T= XP_006714200.1:p.Leu469=
XR_001741172.2:n.1925T=
NM_000128.4:c.1451T= MANE Select NP_000119.1:p.Leu484=