Canonical Allele Identifier: CA1519937773

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284165G= , CM000666.2:g.186284165G=	GRCh38
NC_000004.11:g.187205319G= , CM000666.1:g.187205319G=	GRCh37
NC_000004.10:g.187442313G=	NCBI36
NG_008051.1:g.23202G= , LRG_583:g.23202G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1209G= MANE Select	ENSP00000384957.2:p.Val403=
ENST00000264692.8:c.1047G=	ENSP00000264692.5:p.Val349=
ENST00000403665.6:c.1209G=	ENSP00000384957.2:p.Val403=
NM_000128.3:c.1209G= , LRG_583t1:c.1209G=	NP_000119.1:p.Val403=
XM_005262821.2:c.1212G=	XP_005262878.1:p.Val404=
XM_005262822.2:c.1212G=	XP_005262879.1:p.Val404=
XM_005262823.2:c.942G=	XP_005262880.1:p.Val314=
XM_005262824.1:c.1212G=	XP_005262881.1:p.Val404=
XM_006714137.1:c.1164G=	XP_006714200.1:p.Val388=
XR_938706.1:n.1617G=
XR_938707.1:n.1617G=
XM_005262821.4:c.1212G=	XP_005262878.1:p.Val404=
XM_005262822.4:c.1212G=	XP_005262879.1:p.Val404=
XM_005262823.4:c.942G=	XP_005262880.1:p.Val314=
XM_006714137.3:c.1164G=	XP_006714200.1:p.Val388=
XM_017007884.2:c.*2181G=	XP_016863373.1:n.*2181G=
XM_017007885.2:c.*77G=	XP_016863374.1:n.*77G=
XR_001741172.2:n.1683G=
NM_000128.4:c.1209G= MANE Select	NP_000119.1:p.Val403=