Canonical Allele Identifier: CA1519936018

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186280352A= , CM000666.2:g.186280352A=	GRCh38
NC_000004.11:g.187201506A= , CM000666.1:g.187201506A=	GRCh37
NC_000004.10:g.187438500A=	NCBI36
NG_008051.1:g.19389A= , LRG_583:g.19389A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.995A= MANE Select	ENSP00000384957.2:p.Tyr332=
ENST00000264692.8:c.833A=	ENSP00000264692.5:p.Tyr278=
ENST00000403665.6:c.995A=	ENSP00000384957.2:p.Tyr332=
ENST00000452239.1:c.442A=
NM_000128.3:c.995A= , LRG_583t1:c.995A=	NP_000119.1:p.Tyr332=
XM_005262821.2:c.995A=	XP_005262878.1:p.Tyr332=
XM_005262822.2:c.995A=	XP_005262879.1:p.Tyr332=
XM_005262823.2:c.725A=	XP_005262880.1:p.Tyr242=
XM_005262824.1:c.995A=	XP_005262881.1:p.Tyr332=
XM_006714137.1:c.947A=	XP_006714200.1:p.Tyr316=
XR_938706.1:n.1347A=
XR_938707.1:n.1347A=
XM_005262821.4:c.995A=	XP_005262878.1:p.Tyr332=
XM_005262822.4:c.995A=	XP_005262879.1:p.Tyr332=
XM_005262823.4:c.725A=	XP_005262880.1:p.Tyr242=
XM_006714137.3:c.947A=	XP_006714200.1:p.Tyr316=
XM_017007884.2:c.995A=	XP_016863373.1:p.Tyr332=
XM_017007885.2:c.995A=	XP_016863374.1:p.Tyr332=
XM_017007886.2:c.995A=	XP_016863375.1:p.Tyr332=
XR_001741172.2:n.1328A=
NM_000128.4:c.995A= MANE Select	NP_000119.1:p.Tyr332=