Canonical Allele Identifier: CA1519937787

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284188C= , CM000666.2:g.186284188C=	GRCh38
NC_000004.11:g.187205342C= , CM000666.1:g.187205342C=	GRCh37
NC_000004.10:g.187442336C=	NCBI36
NG_008051.1:g.23225C= , LRG_583:g.23225C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1232C= MANE Select	ENSP00000384957.2:p.Thr411=
ENST00000264692.8:c.1070C=	ENSP00000264692.5:p.Thr357=
ENST00000403665.6:c.1232C=	ENSP00000384957.2:p.Thr411=
NM_000128.3:c.1232C= , LRG_583t1:c.1232C=	NP_000119.1:p.Thr411=
XM_005262821.2:c.1235C=	XP_005262878.1:p.Thr412=
XM_005262822.2:c.1235C=	XP_005262879.1:p.Thr412=
XM_005262823.2:c.965C=	XP_005262880.1:p.Thr322=
XM_005262824.1:c.1235C=	XP_005262881.1:p.Thr412=
XM_006714137.1:c.1187C=	XP_006714200.1:p.Thr396=
XR_938706.1:n.1640C=
XR_938707.1:n.1640C=
XM_005262821.4:c.1235C=	XP_005262878.1:p.Thr412=
XM_005262822.4:c.1235C=	XP_005262879.1:p.Thr412=
XM_005262823.4:c.965C=	XP_005262880.1:p.Thr322=
XM_006714137.3:c.1187C=	XP_006714200.1:p.Thr396=
XR_001741172.2:n.1706C=
NM_000128.4:c.1232C= MANE Select	NP_000119.1:p.Thr411=