Canonical Allele Identifier: CA1519937809

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284220G= , CM000666.2:g.186284220G=	GRCh38
NC_000004.11:g.187205374G= , CM000666.1:g.187205374G=	GRCh37
NC_000004.10:g.187442368G=	NCBI36
NG_008051.1:g.23257G= , LRG_583:g.23257G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1264G= MANE Select	ENSP00000384957.2:p.Gly422=
ENST00000264692.8:c.1102G=	ENSP00000264692.5:p.Gly368=
ENST00000403665.6:c.1264G=	ENSP00000384957.2:p.Gly422=
NM_000128.3:c.1264G= , LRG_583t1:c.1264G=	NP_000119.1:p.Gly422=
XM_005262821.2:c.1267G=	XP_005262878.1:p.Gly423=
XM_005262822.2:c.1267G=	XP_005262879.1:p.Gly423=
XM_005262823.2:c.997G=	XP_005262880.1:p.Gly333=
XM_005262824.1:c.1267G=	XP_005262881.1:p.Gly423=
XM_006714137.1:c.1219G=	XP_006714200.1:p.Gly407=
XR_938706.1:n.1672G=
XR_938707.1:n.1672G=
XM_005262821.4:c.1267G=	XP_005262878.1:p.Gly423=
XM_005262822.4:c.1267G=	XP_005262879.1:p.Gly423=
XM_005262823.4:c.997G=	XP_005262880.1:p.Gly333=
XM_006714137.3:c.1219G=	XP_006714200.1:p.Gly407=
XR_001741172.2:n.1738G=
NM_000128.4:c.1264G= MANE Select	NP_000119.1:p.Gly422=