Canonical Allele Identifier: CA1519937805

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284215T= , CM000666.2:g.186284215T=	GRCh38
NC_000004.11:g.187205369T= , CM000666.1:g.187205369T=	GRCh37
NC_000004.10:g.187442363T=	NCBI36
NG_008051.1:g.23252T= , LRG_583:g.23252T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1259T= MANE Select	ENSP00000384957.2:p.Ile420=
ENST00000264692.8:c.1097T=	ENSP00000264692.5:p.Ile366=
ENST00000403665.6:c.1259T=	ENSP00000384957.2:p.Ile420=
NM_000128.3:c.1259T= , LRG_583t1:c.1259T=	NP_000119.1:p.Ile420=
XM_005262821.2:c.1262T=	XP_005262878.1:p.Ile421=
XM_005262822.2:c.1262T=	XP_005262879.1:p.Ile421=
XM_005262823.2:c.992T=	XP_005262880.1:p.Ile331=
XM_005262824.1:c.1262T=	XP_005262881.1:p.Ile421=
XM_006714137.1:c.1214T=	XP_006714200.1:p.Ile405=
XR_938706.1:n.1667T=
XR_938707.1:n.1667T=
XM_005262821.4:c.1262T=	XP_005262878.1:p.Ile421=
XM_005262822.4:c.1262T=	XP_005262879.1:p.Ile421=
XM_005262823.4:c.992T=	XP_005262880.1:p.Ile331=
XM_006714137.3:c.1214T=	XP_006714200.1:p.Ile405=
XR_001741172.2:n.1733T=
NM_000128.4:c.1259T= MANE Select	NP_000119.1:p.Ile420=