Canonical Allele Identifier: CA1519936013

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186280341G= , CM000666.2:g.186280341G=	GRCh38
NC_000004.11:g.187201495G= , CM000666.1:g.187201495G=	GRCh37
NC_000004.10:g.187438489G=	NCBI36
NG_008051.1:g.19378G= , LRG_583:g.19378G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.984G= MANE Select	ENSP00000384957.2:p.Gln328=
ENST00000264692.8:c.822G=	ENSP00000264692.5:p.Gln274=
ENST00000403665.6:c.984G=	ENSP00000384957.2:p.Gln328=
ENST00000452239.1:c.431G=
NM_000128.3:c.984G= , LRG_583t1:c.984G=	NP_000119.1:p.Gln328=
XM_005262821.2:c.984G=	XP_005262878.1:p.Gln328=
XM_005262822.2:c.984G=	XP_005262879.1:p.Gln328=
XM_005262823.2:c.714G=	XP_005262880.1:p.Gln238=
XM_005262824.1:c.984G=	XP_005262881.1:p.Gln328=
XM_006714137.1:c.936G=	XP_006714200.1:p.Gln312=
XR_938706.1:n.1336G=
XR_938707.1:n.1336G=
XM_005262821.4:c.984G=	XP_005262878.1:p.Gln328=
XM_005262822.4:c.984G=	XP_005262879.1:p.Gln328=
XM_005262823.4:c.714G=	XP_005262880.1:p.Gln238=
XM_006714137.3:c.936G=	XP_006714200.1:p.Gln312=
XM_017007884.2:c.984G=	XP_016863373.1:p.Gln328=
XM_017007885.2:c.984G=	XP_016863374.1:p.Gln328=
XM_017007886.2:c.984G=	XP_016863375.1:p.Gln328=
XR_001741172.2:n.1317G=
NM_000128.4:c.984G= MANE Select	NP_000119.1:p.Gln328=