Canonical Allele Identifier: CA1071927093

Gene: F11

Linked Data

• dbSNP Id: rs1741049912
• gnomAD v3: 4-186284575-G-GAA
• gnomAD v4: 4-186284575-G-GAA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284576_186284577dup , CM000666.2:g.186284576_186284577dup	GRCh38
NC_000004.11:g.187205730_187205731dup , CM000666.1:g.187205730_187205731dup	GRCh37
NC_000004.10:g.187442724_187442725dup	NCBI36
NG_008051.1:g.23613_23614dup , LRG_583:g.23613_23614dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1304+316_1304+317dup MANE Select	ENSP00000384957.2:n.1304+316_1304+317dup
ENST00000264692.8:c.1142+316_1142+317dup	ENSP00000264692.5:n.1142+316_1142+317dup
ENST00000403665.6:c.1304+316_1304+317dup	ENSP00000384957.2:n.1304+316_1304+317dup
NM_000128.3:c.1304+316_1304+317dup , LRG_583t1:c.1304+316_1304+317dup	NP_000119.1:n.1304+316_1304+317dup
XM_005262821.2:c.1307+316_1307+317dup	XP_005262878.1:n.1307+316_1307+317dup
XM_005262822.2:c.1307+316_1307+317dup	XP_005262879.1:n.1307+316_1307+317dup
XM_005262823.2:c.1037+316_1037+317dup	XP_005262880.1:n.1037+316_1037+317dup
XM_005262824.1:c.1307+316_1307+317dup	XP_005262881.1:n.1307+316_1307+317dup
XM_006714137.1:c.1259+316_1259+317dup	XP_006714200.1:n.1259+316_1259+317dup
XR_938706.1:n.1712+316_1712+317dup
XR_938707.1:n.1712+316_1712+317dup
XM_005262821.4:c.1307+316_1307+317dup	XP_005262878.1:n.1307+316_1307+317dup
XM_005262822.4:c.1307+316_1307+317dup	XP_005262879.1:n.1307+316_1307+317dup
XM_005262823.4:c.1037+316_1037+317dup	XP_005262880.1:n.1037+316_1037+317dup
XM_006714137.3:c.1259+316_1259+317dup	XP_006714200.1:n.1259+316_1259+317dup
XR_001741172.2:n.1778+316_1778+317dup
NM_000128.4:c.1304+316_1304+317dup MANE Select	NP_000119.1:n.1304+316_1304+317dup