Canonical Allele Identifier: CA1519937746

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284121G= , CM000666.2:g.186284121G=	GRCh38
NC_000004.11:g.187205275G= , CM000666.1:g.187205275G=	GRCh37
NC_000004.10:g.187442269G=	NCBI36
NG_008051.1:g.23158G= , LRG_583:g.23158G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1165G= MANE Select	ENSP00000384957.2:p.Val389=
ENST00000264692.8:c.1003G=	ENSP00000264692.5:p.Val335=
ENST00000403665.6:c.1165G=	ENSP00000384957.2:p.Val389=
NM_000128.3:c.1165G= , LRG_583t1:c.1165G=	NP_000119.1:p.Val389=
XM_005262821.2:c.1168G=	XP_005262878.1:p.Val390=
XM_005262822.2:c.1168G=	XP_005262879.1:p.Val390=
XM_005262823.2:c.898G=	XP_005262880.1:p.Val300=
XM_005262824.1:c.1168G=	XP_005262881.1:p.Val390=
XM_006714137.1:c.1120G=	XP_006714200.1:p.Val374=
XR_938706.1:n.1573G=
XR_938707.1:n.1573G=
XM_005262821.4:c.1168G=	XP_005262878.1:p.Val390=
XM_005262822.4:c.1168G=	XP_005262879.1:p.Val390=
XM_005262823.4:c.898G=	XP_005262880.1:p.Val300=
XM_006714137.3:c.1120G=	XP_006714200.1:p.Val374=
XM_017007884.2:c.*2137G=	XP_016863373.1:n.*2137G=
XM_017007885.2:c.*33G=	XP_016863374.1:n.*33G=
XR_001741172.2:n.1639G=
NM_000128.4:c.1165G= MANE Select	NP_000119.1:p.Val389=