Canonical Allele Identifier: CA1519938515

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186285709C= , CM000666.2:g.186285709C=	GRCh38
NC_000004.11:g.187206863C= , CM000666.1:g.187206863C=	GRCh37
NC_000004.10:g.187443857C=	NCBI36
NG_008051.1:g.24746C= , LRG_583:g.24746C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1376C= MANE Select	ENSP00000384957.2:p.Ser459=
ENST00000264691.4:c.72C=
ENST00000264692.8:c.1214C=	ENSP00000264692.5:p.Ser405=
ENST00000403665.6:c.1376C=	ENSP00000384957.2:p.Ser459=
NM_000128.3:c.1376C= , LRG_583t1:c.1376C=	NP_000119.1:p.Ser459=
XM_005262821.2:c.1379C=	XP_005262878.1:p.Ser460=
XM_005262822.2:c.1379C=	XP_005262879.1:p.Ser460=
XM_005262823.2:c.1109C=	XP_005262880.1:p.Ser370=
XM_005262824.1:c.1379C=	XP_005262881.1:p.Ser460=
XM_006714137.1:c.1331C=	XP_006714200.1:p.Ser444=
XR_938706.1:n.1784C=
XR_938707.1:n.1784C=
XM_005262821.4:c.1379C=	XP_005262878.1:p.Ser460=
XM_005262822.4:c.1379C=	XP_005262879.1:p.Ser460=
XM_005262823.4:c.1109C=	XP_005262880.1:p.Ser370=
XM_006714137.3:c.1331C=	XP_006714200.1:p.Ser444=
XR_001741172.2:n.1850C=
NM_000128.4:c.1376C= MANE Select	NP_000119.1:p.Ser459=