Canonical Allele Identifier: CA1519937820

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284241G= , CM000666.2:g.186284241G=	GRCh38
NC_000004.11:g.187205395G= , CM000666.1:g.187205395G=	GRCh37
NC_000004.10:g.187442389G=	NCBI36
NG_008051.1:g.23278G= , LRG_583:g.23278G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1285G= MANE Select	ENSP00000384957.2:p.Ala429=
ENST00000264692.8:c.1123G=	ENSP00000264692.5:p.Ala375=
ENST00000403665.6:c.1285G=	ENSP00000384957.2:p.Ala429=
NM_000128.3:c.1285G= , LRG_583t1:c.1285G=	NP_000119.1:p.Ala429=
XM_005262821.2:c.1288G=	XP_005262878.1:p.Ala430=
XM_005262822.2:c.1288G=	XP_005262879.1:p.Ala430=
XM_005262823.2:c.1018G=	XP_005262880.1:p.Ala340=
XM_005262824.1:c.1288G=	XP_005262881.1:p.Ala430=
XM_006714137.1:c.1240G=	XP_006714200.1:p.Ala414=
XR_938706.1:n.1693G=
XR_938707.1:n.1693G=
XM_005262821.4:c.1288G=	XP_005262878.1:p.Ala430=
XM_005262822.4:c.1288G=	XP_005262879.1:p.Ala430=
XM_005262823.4:c.1018G=	XP_005262880.1:p.Ala340=
XM_006714137.3:c.1240G=	XP_006714200.1:p.Ala414=
XR_001741172.2:n.1759G=
NM_000128.4:c.1285G= MANE Select	NP_000119.1:p.Ala429=