Canonical Allele Identifier: CA1519936110

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186280515_186280517delinsCTA , CM000666.2:g.186280515_186280517delinsCTA	GRCh38
NC_000004.11:g.187201669_187201671delinsCTA , CM000666.1:g.187201669_187201671delinsCTA	GRCh37
NC_000004.10:g.187438663_187438665delinsCTA	NCBI36
NG_008051.1:g.19552_19554delinsCTA , LRG_583:g.19552_19554delinsCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1070_1072delinsCTA MANE Select	ENSP00000384957.2:p.Thr357=
ENST00000264692.8:c.908_910delinsCTA	ENSP00000264692.5:p.Thr303=
ENST00000403665.6:c.1070_1072delinsCTA	ENSP00000384957.2:p.Thr357=
ENST00000452239.1:c.517_519delinsCTA
NM_000128.3:c.1070_1072delinsCTA , LRG_583t1:c.1070_1072delinsCTA	NP_000119.1:p.Thr357=
XM_005262821.2:c.1073_1075delinsCTA	XP_005262878.1:p.Thr358=
XM_005262822.2:c.1073_1075delinsCTA	XP_005262879.1:p.Thr358=
XM_005262823.2:c.803_805delinsCTA	XP_005262880.1:p.Thr268=
XM_005262824.1:c.1073_1075delinsCTA	XP_005262881.1:p.Thr358=
XM_006714137.1:c.1025_1027delinsCTA	XP_006714200.1:p.Thr342=
XR_938706.1:n.1425_1427delinsCTA
XR_938707.1:n.1425_1427delinsCTA
XM_005262821.4:c.1073_1075delinsCTA	XP_005262878.1:p.Thr358=
XM_005262822.4:c.1073_1075delinsCTA	XP_005262879.1:p.Thr358=
XM_005262823.4:c.803_805delinsCTA	XP_005262880.1:p.Thr268=
XM_006714137.3:c.1025_1027delinsCTA	XP_006714200.1:p.Thr342=
XM_017007884.2:c.1073_1075delinsCTA	XP_016863373.1:p.Thr358=
XM_017007885.2:c.1073_1075delinsCTA	XP_016863374.1:p.Thr358=
XM_017007886.2:c.1070_1072delinsCTA	XP_016863375.1:p.Thr357=
XR_001741172.2:n.1491_1493delinsCTA
NM_000128.4:c.1070_1072delinsCTA MANE Select	NP_000119.1:p.Thr357=