Canonical Allele Identifier: CA1519934209

Gene: F11

Linked Data

• dbSNP Id: rs761543485

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186276343_186276346dup , CM000666.2:g.186276343_186276346dup	GRCh38
NC_000004.11:g.187197497_187197500dup , CM000666.1:g.187197497_187197500dup	GRCh37
NC_000004.10:g.187434491_187434494dup	NCBI36
NG_008051.1:g.15380_15383dup , LRG_583:g.15380_15383dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.708_711dup MANE Select	ENSP00000384957.2:p.Phe238LeufsTer22
ENST00000264692.8:c.546_549dup	ENSP00000264692.5:p.Phe184LeufsTer22
ENST00000403665.6:c.708_711dup	ENSP00000384957.2:p.Phe238LeufsTer22
ENST00000452239.1:c.155_158dup
NM_000128.3:c.708_711dup , LRG_583t1:c.708_711dup	NP_000119.1:p.Phe238LeufsTer22
XM_005262821.2:c.708_711dup	XP_005262878.1:p.Phe238LeufsTer22
XM_005262822.2:c.708_711dup	XP_005262879.1:p.Phe238LeufsTer22
XM_005262823.2:c.485+2068_485+2071dup	XP_005262880.1:n.485+2068_485+2071dup
XM_005262824.1:c.708_711dup	XP_005262881.1:p.Phe238LeufsTer22
XM_006714137.1:c.708_711dup	XP_006714200.1:p.Phe238LeufsTer22
XR_938706.1:n.1060_1063dup
XR_938707.1:n.1060_1063dup
XM_005262821.4:c.708_711dup	XP_005262878.1:p.Phe238LeufsTer22
XM_005262822.4:c.708_711dup	XP_005262879.1:p.Phe238LeufsTer22
XM_005262823.4:c.485+2068_485+2071dup	XP_005262880.1:n.485+2068_485+2071dup
XM_006714137.3:c.708_711dup	XP_006714200.1:p.Phe238LeufsTer22
XM_017007884.2:c.708_711dup	XP_016863373.1:p.Phe238LeufsTer22
XM_017007885.2:c.708_711dup	XP_016863374.1:p.Phe238LeufsTer22
XM_017007886.2:c.708_711dup	XP_016863375.1:p.Phe238LeufsTer22
XR_001741172.2:n.1041_1044dup
NM_000128.4:c.708_711dup MANE Select	NP_000119.1:p.Phe238LeufsTer22