Canonical Allele Identifier: CA1519937768

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284157T= , CM000666.2:g.186284157T=	GRCh38
NC_000004.11:g.187205311T= , CM000666.1:g.187205311T=	GRCh37
NC_000004.10:g.187442305T=	NCBI36
NG_008051.1:g.23194T= , LRG_583:g.23194T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1201T= MANE Select	ENSP00000384957.2:p.Trp401=
ENST00000264692.8:c.1039T=	ENSP00000264692.5:p.Trp347=
ENST00000403665.6:c.1201T=	ENSP00000384957.2:p.Trp401=
NM_000128.3:c.1201T= , LRG_583t1:c.1201T=	NP_000119.1:p.Trp401=
XM_005262821.2:c.1204T=	XP_005262878.1:p.Trp402=
XM_005262822.2:c.1204T=	XP_005262879.1:p.Trp402=
XM_005262823.2:c.934T=	XP_005262880.1:p.Trp312=
XM_005262824.1:c.1204T=	XP_005262881.1:p.Trp402=
XM_006714137.1:c.1156T=	XP_006714200.1:p.Trp386=
XR_938706.1:n.1609T=
XR_938707.1:n.1609T=
XM_005262821.4:c.1204T=	XP_005262878.1:p.Trp402=
XM_005262822.4:c.1204T=	XP_005262879.1:p.Trp402=
XM_005262823.4:c.934T=	XP_005262880.1:p.Trp312=
XM_006714137.3:c.1156T=	XP_006714200.1:p.Trp386=
XM_017007884.2:c.*2173T=	XP_016863373.1:n.*2173T=
XM_017007885.2:c.*69T=	XP_016863374.1:n.*69T=
XR_001741172.2:n.1675T=
NM_000128.4:c.1201T= MANE Select	NP_000119.1:p.Trp401=