Canonical Allele Identifier: CA1519937780

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284178A= , CM000666.2:g.186284178A=	GRCh38
NC_000004.11:g.187205332A= , CM000666.1:g.187205332A=	GRCh37
NC_000004.10:g.187442326A=	NCBI36
NG_008051.1:g.23215A= , LRG_583:g.23215A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1222A= MANE Select	ENSP00000384957.2:p.Thr408=
ENST00000264692.8:c.1060A=	ENSP00000264692.5:p.Thr354=
ENST00000403665.6:c.1222A=	ENSP00000384957.2:p.Thr408=
NM_000128.3:c.1222A= , LRG_583t1:c.1222A=	NP_000119.1:p.Thr408=
XM_005262821.2:c.1225A=	XP_005262878.1:p.Thr409=
XM_005262822.2:c.1225A=	XP_005262879.1:p.Thr409=
XM_005262823.2:c.955A=	XP_005262880.1:p.Thr319=
XM_005262824.1:c.1225A=	XP_005262881.1:p.Thr409=
XM_006714137.1:c.1177A=	XP_006714200.1:p.Thr393=
XR_938706.1:n.1630A=
XR_938707.1:n.1630A=
XM_005262821.4:c.1225A=	XP_005262878.1:p.Thr409=
XM_005262822.4:c.1225A=	XP_005262879.1:p.Thr409=
XM_005262823.4:c.955A=	XP_005262880.1:p.Thr319=
XM_006714137.3:c.1177A=	XP_006714200.1:p.Thr393=
XM_017007884.2:c.*2194A=	XP_016863373.1:n.*2194A=
XR_001741172.2:n.1696A=
NM_000128.4:c.1222A= MANE Select	NP_000119.1:p.Thr408=