Canonical Allele Identifier: CA1519938546
Gene: F11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186285785G= , CM000666.2:g.186285785G= GRCh38
NC_000004.11:g.187206939G= , CM000666.1:g.187206939G= GRCh37
NC_000004.10:g.187443933G= NCBI36
NG_008051.1:g.24822G= , LRG_583:g.24822G=

Transcript Alleles

HGVS Amino-acid change
ENST00000403665.7:c.1452G= MANE Select ENSP00000384957.2:p.Leu484=
ENST00000264691.4:c.148G=
ENST00000264692.8:c.1290G= ENSP00000264692.5:p.Leu430=
ENST00000403665.6:c.1452G= ENSP00000384957.2:p.Leu484=
NM_000128.3:c.1452G= , LRG_583t1:c.1452G= NP_000119.1:p.Leu484=
XM_005262821.2:c.1455G= XP_005262878.1:p.Leu485=
XM_005262822.2:c.1455G= XP_005262879.1:p.Leu485=
XM_005262823.2:c.1185G= XP_005262880.1:p.Leu395=
XM_005262824.1:c.1455G= XP_005262881.1:p.Leu485=
XM_006714137.1:c.1407G= XP_006714200.1:p.Leu469=
XR_938706.1:n.1860G=
XR_938707.1:n.1860G=
XM_005262821.4:c.1455G= XP_005262878.1:p.Leu485=
XM_005262822.4:c.1455G= XP_005262879.1:p.Leu485=
XM_005262823.4:c.1185G= XP_005262880.1:p.Leu395=
XM_006714137.3:c.1407G= XP_006714200.1:p.Leu469=
XR_001741172.2:n.1926G=
NM_000128.4:c.1452G= MANE Select NP_000119.1:p.Leu484=