Canonical Allele Identifier: CA1519938532

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186285749T= , CM000666.2:g.186285749T=	GRCh38
NC_000004.11:g.187206903T= , CM000666.1:g.187206903T=	GRCh37
NC_000004.10:g.187443897T=	NCBI36
NG_008051.1:g.24786T= , LRG_583:g.24786T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1416T= MANE Select	ENSP00000384957.2:p.Tyr472=
ENST00000264691.4:c.112T=
ENST00000264692.8:c.1254T=	ENSP00000264692.5:p.Tyr418=
ENST00000403665.6:c.1416T=	ENSP00000384957.2:p.Tyr472=
NM_000128.3:c.1416T= , LRG_583t1:c.1416T=	NP_000119.1:p.Tyr472=
XM_005262821.2:c.1419T=	XP_005262878.1:p.Tyr473=
XM_005262822.2:c.1419T=	XP_005262879.1:p.Tyr473=
XM_005262823.2:c.1149T=	XP_005262880.1:p.Tyr383=
XM_005262824.1:c.1419T=	XP_005262881.1:p.Tyr473=
XM_006714137.1:c.1371T=	XP_006714200.1:p.Tyr457=
XR_938706.1:n.1824T=
XR_938707.1:n.1824T=
XM_005262821.4:c.1419T=	XP_005262878.1:p.Tyr473=
XM_005262822.4:c.1419T=	XP_005262879.1:p.Tyr473=
XM_005262823.4:c.1149T=	XP_005262880.1:p.Tyr383=
XM_006714137.3:c.1371T=	XP_006714200.1:p.Tyr457=
XR_001741172.2:n.1890T=
NM_000128.4:c.1416T= MANE Select	NP_000119.1:p.Tyr472=