Canonical Allele Identifier: CA2672903467

Gene: F11

Linked Data

• gnomAD v4: 4-186284052-A-AAG

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284054_186284055dup , CM000666.2:g.186284054_186284055dup	GRCh38
NC_000004.11:g.187205208_187205209dup , CM000666.1:g.187205208_187205209dup	GRCh37
NC_000004.10:g.187442202_187442203dup	NCBI36
NG_008051.1:g.23091_23092dup , LRG_583:g.23091_23092dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1136-38_1136-37dup MANE Select	ENSP00000384957.2:n.1136-38_1136-37dup
ENST00000264692.8:c.974-38_974-37dup	ENSP00000264692.5:n.974-38_974-37dup
ENST00000403665.6:c.1136-38_1136-37dup	ENSP00000384957.2:n.1136-38_1136-37dup
NM_000128.3:c.1136-38_1136-37dup , LRG_583t1:c.1136-38_1136-37dup	NP_000119.1:n.1136-38_1136-37dup
XM_005262821.2:c.1139-38_1139-37dup	XP_005262878.1:n.1139-38_1139-37dup
XM_005262822.2:c.1139-38_1139-37dup	XP_005262879.1:n.1139-38_1139-37dup
XM_005262823.2:c.869-38_869-37dup	XP_005262880.1:n.869-38_869-37dup
XM_005262824.1:c.1139-38_1139-37dup	XP_005262881.1:n.1139-38_1139-37dup
XM_006714137.1:c.1091-38_1091-37dup	XP_006714200.1:n.1091-38_1091-37dup
XR_938706.1:n.1544-38_1544-37dup
XR_938707.1:n.1544-38_1544-37dup
XM_005262821.4:c.1139-38_1139-37dup	XP_005262878.1:n.1139-38_1139-37dup
XM_005262822.4:c.1139-38_1139-37dup	XP_005262879.1:n.1139-38_1139-37dup
XM_005262823.4:c.869-38_869-37dup	XP_005262880.1:n.869-38_869-37dup
XM_006714137.3:c.1091-38_1091-37dup	XP_006714200.1:n.1091-38_1091-37dup
XM_017007884.2:c.*2070_*2071dup	XP_016863373.1:n.*2070_*2071dup
XM_017007885.2:c.*4-38_*4-37dup	XP_016863374.1:n.*4-38_*4-37dup
XR_001741172.2:n.1610-38_1610-37dup
NM_000128.4:c.1136-38_1136-37dup MANE Select	NP_000119.1:n.1136-38_1136-37dup