Canonical Allele Identifier: CA1519937795

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284200T= , CM000666.2:g.186284200T=	GRCh38
NC_000004.11:g.187205354T= , CM000666.1:g.187205354T=	GRCh37
NC_000004.10:g.187442348T=	NCBI36
NG_008051.1:g.23237T= , LRG_583:g.23237T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1244T= MANE Select	ENSP00000384957.2:p.Leu415=
ENST00000264692.8:c.1082T=	ENSP00000264692.5:p.Leu361=
ENST00000403665.6:c.1244T=	ENSP00000384957.2:p.Leu415=
NM_000128.3:c.1244T= , LRG_583t1:c.1244T=	NP_000119.1:p.Leu415=
XM_005262821.2:c.1247T=	XP_005262878.1:p.Leu416=
XM_005262822.2:c.1247T=	XP_005262879.1:p.Leu416=
XM_005262823.2:c.977T=	XP_005262880.1:p.Leu326=
XM_005262824.1:c.1247T=	XP_005262881.1:p.Leu416=
XM_006714137.1:c.1199T=	XP_006714200.1:p.Leu400=
XR_938706.1:n.1652T=
XR_938707.1:n.1652T=
XM_005262821.4:c.1247T=	XP_005262878.1:p.Leu416=
XM_005262822.4:c.1247T=	XP_005262879.1:p.Leu416=
XM_005262823.4:c.977T=	XP_005262880.1:p.Leu326=
XM_006714137.3:c.1199T=	XP_006714200.1:p.Leu400=
XR_001741172.2:n.1718T=
NM_000128.4:c.1244T= MANE Select	NP_000119.1:p.Leu415=