Canonical Allele Identifier: CA2578250235

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186276353dup , CM000666.2:g.186276353dup	GRCh38
NC_000004.11:g.187197507dup , CM000666.1:g.187197507dup	GRCh37
NC_000004.10:g.187434501dup	NCBI36
NG_008051.1:g.15390dup , LRG_583:g.15390dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.718dup MANE Select	ENSP00000384957.2:p.Thr240AsnfsTer19
ENST00000264692.8:c.556dup	ENSP00000264692.5:p.Thr186AsnfsTer19
ENST00000403665.6:c.718dup	ENSP00000384957.2:p.Thr240AsnfsTer19
ENST00000452239.1:c.165dup
NM_000128.3:c.718dup , LRG_583t1:c.718dup	NP_000119.1:p.Thr240AsnfsTer19
XM_005262821.2:c.718dup	XP_005262878.1:p.Thr240AsnfsTer19
XM_005262822.2:c.718dup	XP_005262879.1:p.Thr240AsnfsTer19
XM_005262823.2:c.485+2078dup	XP_005262880.1:n.485+2078dup
XM_005262824.1:c.718dup	XP_005262881.1:p.Thr240AsnfsTer19
XM_006714137.1:c.718dup	XP_006714200.1:p.Thr240AsnfsTer19
XR_938706.1:n.1070dup
XR_938707.1:n.1070dup
XM_005262821.4:c.718dup	XP_005262878.1:p.Thr240AsnfsTer19
XM_005262822.4:c.718dup	XP_005262879.1:p.Thr240AsnfsTer19
XM_005262823.4:c.485+2078dup	XP_005262880.1:n.485+2078dup
XM_006714137.3:c.718dup	XP_006714200.1:p.Thr240AsnfsTer19
XM_017007884.2:c.718dup	XP_016863373.1:p.Thr240AsnfsTer19
XM_017007885.2:c.718dup	XP_016863374.1:p.Thr240AsnfsTer19
XM_017007886.2:c.718dup	XP_016863375.1:p.Thr240AsnfsTer19
XR_001741172.2:n.1051dup
NM_000128.4:c.718dup MANE Select	NP_000119.1:p.Thr240AsnfsTer19