Canonical Allele Identifier: CA2606976420

Gene: F11

Linked Data

• gnomAD v3: 4-186284642-C-G
• gnomAD v4: 4-186284642-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284642C>G , CM000666.2:g.186284642C>G	GRCh38
NC_000004.11:g.187205796C>G , CM000666.1:g.187205796C>G	GRCh37
NC_000004.10:g.187442790C>G	NCBI36
NG_008051.1:g.23679C>G , LRG_583:g.23679C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1304+382C>G MANE Select	ENSP00000384957.2:n.1304+382C>G
ENST00000264692.8:c.1142+382C>G	ENSP00000264692.5:n.1142+382C>G
ENST00000403665.6:c.1304+382C>G	ENSP00000384957.2:n.1304+382C>G
NM_000128.3:c.1304+382C>G , LRG_583t1:c.1304+382C>G	NP_000119.1:n.1304+382C>G
XM_005262821.2:c.1307+382C>G	XP_005262878.1:n.1307+382C>G
XM_005262822.2:c.1307+382C>G	XP_005262879.1:n.1307+382C>G
XM_005262823.2:c.1037+382C>G	XP_005262880.1:n.1037+382C>G
XM_005262824.1:c.1307+382C>G	XP_005262881.1:n.1307+382C>G
XM_006714137.1:c.1259+382C>G	XP_006714200.1:n.1259+382C>G
XR_938706.1:n.1712+382C>G
XR_938707.1:n.1712+382C>G
XM_005262821.4:c.1307+382C>G	XP_005262878.1:n.1307+382C>G
XM_005262822.4:c.1307+382C>G	XP_005262879.1:n.1307+382C>G
XM_005262823.4:c.1037+382C>G	XP_005262880.1:n.1037+382C>G
XM_006714137.3:c.1259+382C>G	XP_006714200.1:n.1259+382C>G
XR_001741172.2:n.1778+382C>G
NM_000128.4:c.1304+382C>G MANE Select	NP_000119.1:n.1304+382C>G