Canonical Allele Identifier: CA1519938500

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186285673G= , CM000666.2:g.186285673G=	GRCh38
NC_000004.11:g.187206827G= , CM000666.1:g.187206827G=	GRCh37
NC_000004.10:g.187443821G=	NCBI36
NG_008051.1:g.24710G= , LRG_583:g.24710G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1340G= MANE Select	ENSP00000384957.2:p.Gly447=
ENST00000264691.4:c.36G=
ENST00000264692.8:c.1178G=	ENSP00000264692.5:p.Gly393=
ENST00000403665.6:c.1340G=	ENSP00000384957.2:p.Gly447=
NM_000128.3:c.1340G= , LRG_583t1:c.1340G=	NP_000119.1:p.Gly447=
XM_005262821.2:c.1343G=	XP_005262878.1:p.Gly448=
XM_005262822.2:c.1343G=	XP_005262879.1:p.Gly448=
XM_005262823.2:c.1073G=	XP_005262880.1:p.Gly358=
XM_005262824.1:c.1343G=	XP_005262881.1:p.Gly448=
XM_006714137.1:c.1295G=	XP_006714200.1:p.Gly432=
XR_938706.1:n.1748G=
XR_938707.1:n.1748G=
XM_005262821.4:c.1343G=	XP_005262878.1:p.Gly448=
XM_005262822.4:c.1343G=	XP_005262879.1:p.Gly448=
XM_005262823.4:c.1073G=	XP_005262880.1:p.Gly358=
XM_006714137.3:c.1295G=	XP_006714200.1:p.Gly432=
XR_001741172.2:n.1814G=
NM_000128.4:c.1340G= MANE Select	NP_000119.1:p.Gly447=