Canonical Allele Identifier: CA1519937783

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284183A= , CM000666.2:g.186284183A=	GRCh38
NC_000004.11:g.187205337A= , CM000666.1:g.187205337A=	GRCh37
NC_000004.10:g.187442331A=	NCBI36
NG_008051.1:g.23220A= , LRG_583:g.23220A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1227A= MANE Select	ENSP00000384957.2:p.Ser409=
ENST00000264692.8:c.1065A=	ENSP00000264692.5:p.Ser355=
ENST00000403665.6:c.1227A=	ENSP00000384957.2:p.Ser409=
NM_000128.3:c.1227A= , LRG_583t1:c.1227A=	NP_000119.1:p.Ser409=
XM_005262821.2:c.1230A=	XP_005262878.1:p.Ser410=
XM_005262822.2:c.1230A=	XP_005262879.1:p.Ser410=
XM_005262823.2:c.960A=	XP_005262880.1:p.Ser320=
XM_005262824.1:c.1230A=	XP_005262881.1:p.Ser410=
XM_006714137.1:c.1182A=	XP_006714200.1:p.Ser394=
XR_938706.1:n.1635A=
XR_938707.1:n.1635A=
XM_005262821.4:c.1230A=	XP_005262878.1:p.Ser410=
XM_005262822.4:c.1230A=	XP_005262879.1:p.Ser410=
XM_005262823.4:c.960A=	XP_005262880.1:p.Ser320=
XM_006714137.3:c.1182A=	XP_006714200.1:p.Ser394=
XM_017007884.2:c.*2199A=	XP_016863373.1:n.*2199A=
XR_001741172.2:n.1701A=
NM_000128.4:c.1227A= MANE Select	NP_000119.1:p.Ser409=