Canonical Allele Identifier: CA1519936019

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186280354A= , CM000666.2:g.186280354A=	GRCh38
NC_000004.11:g.187201508A= , CM000666.1:g.187201508A=	GRCh37
NC_000004.10:g.187438502A=	NCBI36
NG_008051.1:g.19391A= , LRG_583:g.19391A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.997A= MANE Select	ENSP00000384957.2:p.Thr333=
ENST00000264692.8:c.835A=	ENSP00000264692.5:p.Thr279=
ENST00000403665.6:c.997A=	ENSP00000384957.2:p.Thr333=
ENST00000452239.1:c.444A=
NM_000128.3:c.997A= , LRG_583t1:c.997A=	NP_000119.1:p.Thr333=
XM_005262821.2:c.997A=	XP_005262878.1:p.Thr333=
XM_005262822.2:c.997A=	XP_005262879.1:p.Thr333=
XM_005262823.2:c.727A=	XP_005262880.1:p.Thr243=
XM_005262824.1:c.997A=	XP_005262881.1:p.Thr333=
XM_006714137.1:c.949A=	XP_006714200.1:p.Thr317=
XR_938706.1:n.1349A=
XR_938707.1:n.1349A=
XM_005262821.4:c.997A=	XP_005262878.1:p.Thr333=
XM_005262822.4:c.997A=	XP_005262879.1:p.Thr333=
XM_005262823.4:c.727A=	XP_005262880.1:p.Thr243=
XM_006714137.3:c.949A=	XP_006714200.1:p.Thr317=
XM_017007884.2:c.997A=	XP_016863373.1:p.Thr333=
XM_017007885.2:c.997A=	XP_016863374.1:p.Thr333=
XM_017007886.2:c.997A=	XP_016863375.1:p.Thr333=
XR_001741172.2:n.1330A=
NM_000128.4:c.997A= MANE Select	NP_000119.1:p.Thr333=