Canonical Allele Identifier: CA1519938520

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186285723C= , CM000666.2:g.186285723C=	GRCh38
NC_000004.11:g.187206877C= , CM000666.1:g.187206877C=	GRCh37
NC_000004.10:g.187443871C=	NCBI36
NG_008051.1:g.24760C= , LRG_583:g.24760C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000128.4:c.1390C= MANE Select	NP_000119.1:p.Gln464=
ENST00000403665.7:c.1390C= MANE Select	ENSP00000384957.2:p.Gln464=
NM_000128.3:c.1390C= , LRG_583t1:c.1390C=	NP_000119.1:p.Gln464=
ENST00000264691.4:c.86C=
ENST00000264692.8:c.1228C=	ENSP00000264692.5:p.Gln410=
ENST00000403665.6:c.1390C=	ENSP00000384957.2:p.Gln464=
XM_005262821.2:c.1393C=	XP_005262878.1:p.Gln465=
XM_005262821.4:c.1393C=	XP_005262878.1:p.Gln465=
XM_005262822.2:c.1393C=	XP_005262879.1:p.Gln465=
XM_005262822.4:c.1393C=	XP_005262879.1:p.Gln465=
XM_005262823.2:c.1123C=	XP_005262880.1:p.Gln375=
XM_005262823.4:c.1123C=	XP_005262880.1:p.Gln375=
XM_005262824.1:c.1393C=	XP_005262881.1:p.Gln465=
XM_006714137.1:c.1345C=	XP_006714200.1:p.Gln449=
XM_006714137.3:c.1345C=	XP_006714200.1:p.Gln449=
XR_001741172.2:n.1864C=
XR_938706.1:n.1798C=
XR_938707.1:n.1798C=