Canonical Allele Identifier: CA1519937647

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186283931T= , CM000666.2:g.186283931T=	GRCh38
NC_000004.11:g.187205085T= , CM000666.1:g.187205085T=	GRCh37
NC_000004.10:g.187442079T=	NCBI36
NG_008051.1:g.22968T= , LRG_583:g.22968T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1136-161T= MANE Select	ENSP00000384957.2:n.1136-161T=
ENST00000264692.8:c.974-161T=	ENSP00000264692.5:n.974-161T=
ENST00000403665.6:c.1136-161T=	ENSP00000384957.2:n.1136-161T=
NM_000128.3:c.1136-161T= , LRG_583t1:c.1136-161T=	NP_000119.1:n.1136-161T=
XM_005262821.2:c.1139-161T=	XP_005262878.1:n.1139-161T=
XM_005262822.2:c.1139-161T=	XP_005262879.1:n.1139-161T=
XM_005262823.2:c.869-161T=	XP_005262880.1:n.869-161T=
XM_005262824.1:c.1139-161T=	XP_005262881.1:n.1139-161T=
XM_006714137.1:c.1091-161T=	XP_006714200.1:n.1091-161T=
XR_938706.1:n.1544-161T=
XR_938707.1:n.1544-161T=
XM_005262821.4:c.1139-161T=	XP_005262878.1:n.1139-161T=
XM_005262822.4:c.1139-161T=	XP_005262879.1:n.1139-161T=
XM_005262823.4:c.869-161T=	XP_005262880.1:n.869-161T=
XM_006714137.3:c.1091-161T=	XP_006714200.1:n.1091-161T=
XM_017007884.2:c.*1947T=	XP_016863373.1:n.*1947T=
XM_017007885.2:c.*4-161T=	XP_016863374.1:n.*4-161T=
XR_001741172.2:n.1610-161T=
NM_000128.4:c.1136-161T= MANE Select	NP_000119.1:n.1136-161T=