Canonical Allele Identifier: CA1519937743

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284115A= , CM000666.2:g.186284115A=	GRCh38
NC_000004.11:g.187205269A= , CM000666.1:g.187205269A=	GRCh37
NC_000004.10:g.187442263A=	NCBI36
NG_008051.1:g.23152A= , LRG_583:g.23152A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1159A= MANE Select	ENSP00000384957.2:p.Arg387=
ENST00000264692.8:c.997A=	ENSP00000264692.5:p.Arg333=
ENST00000403665.6:c.1159A=	ENSP00000384957.2:p.Arg387=
NM_000128.3:c.1159A= , LRG_583t1:c.1159A=	NP_000119.1:p.Arg387=
XM_005262821.2:c.1162A=	XP_005262878.1:p.Arg388=
XM_005262822.2:c.1162A=	XP_005262879.1:p.Arg388=
XM_005262823.2:c.892A=	XP_005262880.1:p.Arg298=
XM_005262824.1:c.1162A=	XP_005262881.1:p.Arg388=
XM_006714137.1:c.1114A=	XP_006714200.1:p.Arg372=
XR_938706.1:n.1567A=
XR_938707.1:n.1567A=
XM_005262821.4:c.1162A=	XP_005262878.1:p.Arg388=
XM_005262822.4:c.1162A=	XP_005262879.1:p.Arg388=
XM_005262823.4:c.892A=	XP_005262880.1:p.Arg298=
XM_006714137.3:c.1114A=	XP_006714200.1:p.Arg372=
XM_017007884.2:c.*2131A=	XP_016863373.1:n.*2131A=
XM_017007885.2:c.*27A=	XP_016863374.1:n.*27A=
XR_001741172.2:n.1633A=
NM_000128.4:c.1159A= MANE Select	NP_000119.1:p.Arg387=