Canonical Allele Identifier: CA1519938525

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186285737C= , CM000666.2:g.186285737C=	GRCh38
NC_000004.11:g.187206891C= , CM000666.1:g.187206891C=	GRCh37
NC_000004.10:g.187443885C=	NCBI36
NG_008051.1:g.24774C= , LRG_583:g.24774C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1404C= MANE Select	ENSP00000384957.2:p.Ile468=
ENST00000264691.4:c.100C=
ENST00000264692.8:c.1242C=	ENSP00000264692.5:p.Ile414=
ENST00000403665.6:c.1404C=	ENSP00000384957.2:p.Ile468=
NM_000128.3:c.1404C= , LRG_583t1:c.1404C=	NP_000119.1:p.Ile468=
XM_005262821.2:c.1407C=	XP_005262878.1:p.Ile469=
XM_005262822.2:c.1407C=	XP_005262879.1:p.Ile469=
XM_005262823.2:c.1137C=	XP_005262880.1:p.Ile379=
XM_005262824.1:c.1407C=	XP_005262881.1:p.Ile469=
XM_006714137.1:c.1359C=	XP_006714200.1:p.Ile453=
XR_938706.1:n.1812C=
XR_938707.1:n.1812C=
XM_005262821.4:c.1407C=	XP_005262878.1:p.Ile469=
XM_005262822.4:c.1407C=	XP_005262879.1:p.Ile469=
XM_005262823.4:c.1137C=	XP_005262880.1:p.Ile379=
XM_006714137.3:c.1359C=	XP_006714200.1:p.Ile453=
XR_001741172.2:n.1878C=
NM_000128.4:c.1404C= MANE Select	NP_000119.1:p.Ile468=