Canonical Allele Identifier: CA1519938538

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186285774_186285775delinsAT , CM000666.2:g.186285774_186285775delinsAT	GRCh38
NC_000004.11:g.187206928_187206929delinsAT , CM000666.1:g.187206928_187206929delinsAT	GRCh37
NC_000004.10:g.187443922_187443923delinsAT	NCBI36
NG_008051.1:g.24811_24812delinsAT , LRG_583:g.24811_24812delinsAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1441_1442delinsAT MANE Select	ENSP00000384957.2:p.Ile481=
ENST00000264691.4:c.137_138delinsAT
ENST00000264692.8:c.1279_1280delinsAT	ENSP00000264692.5:p.Ile427=
ENST00000403665.6:c.1441_1442delinsAT	ENSP00000384957.2:p.Ile481=
NM_000128.3:c.1441_1442delinsAT , LRG_583t1:c.1441_1442delinsAT	NP_000119.1:p.Ile481=
XM_005262821.2:c.1444_1445delinsAT	XP_005262878.1:p.Ile482=
XM_005262822.2:c.1444_1445delinsAT	XP_005262879.1:p.Ile482=
XM_005262823.2:c.1174_1175delinsAT	XP_005262880.1:p.Ile392=
XM_005262824.1:c.1444_1445delinsAT	XP_005262881.1:p.Ile482=
XM_006714137.1:c.1396_1397delinsAT	XP_006714200.1:p.Ile466=
XR_938706.1:n.1849_1850delinsAT
XR_938707.1:n.1849_1850delinsAT
XM_005262821.4:c.1444_1445delinsAT	XP_005262878.1:p.Ile482=
XM_005262822.4:c.1444_1445delinsAT	XP_005262879.1:p.Ile482=
XM_005262823.4:c.1174_1175delinsAT	XP_005262880.1:p.Ile392=
XM_006714137.3:c.1396_1397delinsAT	XP_006714200.1:p.Ile466=
XR_001741172.2:n.1915_1916delinsAT
NM_000128.4:c.1441_1442delinsAT MANE Select	NP_000119.1:p.Ile481=