Canonical Allele Identifier: CA1519938519

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186285719G= , CM000666.2:g.186285719G=	GRCh38
NC_000004.11:g.187206873G= , CM000666.1:g.187206873G=	GRCh37
NC_000004.10:g.187443867G=	NCBI36
NG_008051.1:g.24756G= , LRG_583:g.24756G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1386G= MANE Select	ENSP00000384957.2:p.Gly462=
ENST00000264691.4:c.82G=
ENST00000264692.8:c.1224G=	ENSP00000264692.5:p.Gly408=
ENST00000403665.6:c.1386G=	ENSP00000384957.2:p.Gly462=
NM_000128.3:c.1386G= , LRG_583t1:c.1386G=	NP_000119.1:p.Gly462=
XM_005262821.2:c.1389G=	XP_005262878.1:p.Gly463=
XM_005262822.2:c.1389G=	XP_005262879.1:p.Gly463=
XM_005262823.2:c.1119G=	XP_005262880.1:p.Gly373=
XM_005262824.1:c.1389G=	XP_005262881.1:p.Gly463=
XM_006714137.1:c.1341G=	XP_006714200.1:p.Gly447=
XR_938706.1:n.1794G=
XR_938707.1:n.1794G=
XM_005262821.4:c.1389G=	XP_005262878.1:p.Gly463=
XM_005262822.4:c.1389G=	XP_005262879.1:p.Gly463=
XM_005262823.4:c.1119G=	XP_005262880.1:p.Gly373=
XM_006714137.3:c.1341G=	XP_006714200.1:p.Gly447=
XR_001741172.2:n.1860G=
NM_000128.4:c.1386G= MANE Select	NP_000119.1:p.Gly462=