Canonical Allele Identifier: CA1519934194

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186276317C= , CM000666.2:g.186276317C=	GRCh38
NC_000004.11:g.187197471C= , CM000666.1:g.187197471C=	GRCh37
NC_000004.10:g.187434465C=	NCBI36
NG_008051.1:g.15354C= , LRG_583:g.15354C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.682C= MANE Select	ENSP00000384957.2:p.Arg228=
ENST00000264692.8:c.520C=	ENSP00000264692.5:p.Arg174=
ENST00000403665.6:c.682C=	ENSP00000384957.2:p.Arg228=
ENST00000452239.1:c.129C=
NM_000128.3:c.682C= , LRG_583t1:c.682C=	NP_000119.1:p.Arg228=
XM_005262821.2:c.682C=	XP_005262878.1:p.Arg228=
XM_005262822.2:c.682C=	XP_005262879.1:p.Arg228=
XM_005262823.2:c.485+2042C=	XP_005262880.1:n.485+2042C=
XM_005262824.1:c.682C=	XP_005262881.1:p.Arg228=
XM_006714137.1:c.682C=	XP_006714200.1:p.Arg228=
XR_938706.1:n.1034C=
XR_938707.1:n.1034C=
XM_005262821.4:c.682C=	XP_005262878.1:p.Arg228=
XM_005262822.4:c.682C=	XP_005262879.1:p.Arg228=
XM_005262823.4:c.485+2042C=	XP_005262880.1:n.485+2042C=
XM_006714137.3:c.682C=	XP_006714200.1:p.Arg228=
XM_017007884.2:c.682C=	XP_016863373.1:p.Arg228=
XM_017007885.2:c.682C=	XP_016863374.1:p.Arg228=
XM_017007886.2:c.682C=	XP_016863375.1:p.Arg228=
XR_001741172.2:n.1015C=
NM_000128.4:c.682C= MANE Select	NP_000119.1:p.Arg228=