Canonical Allele Identifier: CA1519938493

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186285659G= , CM000666.2:g.186285659G=	GRCh38
NC_000004.11:g.187206813G= , CM000666.1:g.187206813G=	GRCh37
NC_000004.10:g.187443807G=	NCBI36
NG_008051.1:g.24696G= , LRG_583:g.24696G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1326G= MANE Select	ENSP00000384957.2:p.Leu442=
ENST00000264691.4:c.22G=
ENST00000264692.8:c.1164G=	ENSP00000264692.5:p.Leu388=
ENST00000403665.6:c.1326G=	ENSP00000384957.2:p.Leu442=
NM_000128.3:c.1326G= , LRG_583t1:c.1326G=	NP_000119.1:p.Leu442=
XM_005262821.2:c.1329G=	XP_005262878.1:p.Leu443=
XM_005262822.2:c.1329G=	XP_005262879.1:p.Leu443=
XM_005262823.2:c.1059G=	XP_005262880.1:p.Leu353=
XM_005262824.1:c.1329G=	XP_005262881.1:p.Leu443=
XM_006714137.1:c.1281G=	XP_006714200.1:p.Leu427=
XR_938706.1:n.1734G=
XR_938707.1:n.1734G=
XM_005262821.4:c.1329G=	XP_005262878.1:p.Leu443=
XM_005262822.4:c.1329G=	XP_005262879.1:p.Leu443=
XM_005262823.4:c.1059G=	XP_005262880.1:p.Leu353=
XM_006714137.3:c.1281G=	XP_006714200.1:p.Leu427=
XR_001741172.2:n.1800G=
NM_000128.4:c.1326G= MANE Select	NP_000119.1:p.Leu442=