Canonical Allele Identifier: CA1519936114

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186280521T= , CM000666.2:g.186280521T=	GRCh38
NC_000004.11:g.187201675T= , CM000666.1:g.187201675T=	GRCh37
NC_000004.10:g.187438669T=	NCBI36
NG_008051.1:g.19558T= , LRG_583:g.19558T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1076T= MANE Select	ENSP00000384957.2:p.Ile359=
ENST00000264692.8:c.914T=	ENSP00000264692.5:p.Ile305=
ENST00000403665.6:c.1076T=	ENSP00000384957.2:p.Ile359=
ENST00000452239.1:c.523T=
NM_000128.3:c.1076T= , LRG_583t1:c.1076T=	NP_000119.1:p.Ile359=
XM_005262821.2:c.1079T=	XP_005262878.1:p.Ile360=
XM_005262822.2:c.1079T=	XP_005262879.1:p.Ile360=
XM_005262823.2:c.809T=	XP_005262880.1:p.Ile270=
XM_005262824.1:c.1079T=	XP_005262881.1:p.Ile360=
XM_006714137.1:c.1031T=	XP_006714200.1:p.Ile344=
XR_938706.1:n.1431T=
XR_938707.1:n.1431T=
XM_005262821.4:c.1079T=	XP_005262878.1:p.Ile360=
XM_005262822.4:c.1079T=	XP_005262879.1:p.Ile360=
XM_005262823.4:c.809T=	XP_005262880.1:p.Ile270=
XM_006714137.3:c.1031T=	XP_006714200.1:p.Ile344=
XM_017007884.2:c.1079T=	XP_016863373.1:p.Ile360=
XM_017007885.2:c.1079T=	XP_016863374.1:p.Ile360=
XM_017007886.2:c.1076T=	XP_016863375.1:p.Ile359=
XR_001741172.2:n.1497T=
NM_000128.4:c.1076T= MANE Select	NP_000119.1:p.Ile359=