Canonical Allele Identifier: CA1071927022

Gene: F11

Linked Data

• dbSNP Id: rs1741035509
• gnomAD v3: 4-186284439-CAG-C
• gnomAD v4: 4-186284439-CAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284440_186284441del , CM000666.2:g.186284440_186284441del	GRCh38
NC_000004.11:g.187205594_187205595del , CM000666.1:g.187205594_187205595del	GRCh37
NC_000004.10:g.187442588_187442589del	NCBI36
NG_008051.1:g.23477_23478del , LRG_583:g.23477_23478del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1304+180_1304+181del MANE Select	ENSP00000384957.2:n.1304+180_1304+181del
ENST00000264692.8:c.1142+180_1142+181del	ENSP00000264692.5:n.1142+180_1142+181del
ENST00000403665.6:c.1304+180_1304+181del	ENSP00000384957.2:n.1304+180_1304+181del
NM_000128.3:c.1304+180_1304+181del , LRG_583t1:c.1304+180_1304+181del	NP_000119.1:n.1304+180_1304+181del
XM_005262821.2:c.1307+180_1307+181del	XP_005262878.1:n.1307+180_1307+181del
XM_005262822.2:c.1307+180_1307+181del	XP_005262879.1:n.1307+180_1307+181del
XM_005262823.2:c.1037+180_1037+181del	XP_005262880.1:n.1037+180_1037+181del
XM_005262824.1:c.1307+180_1307+181del	XP_005262881.1:n.1307+180_1307+181del
XM_006714137.1:c.1259+180_1259+181del	XP_006714200.1:n.1259+180_1259+181del
XR_938706.1:n.1712+180_1712+181del
XR_938707.1:n.1712+180_1712+181del
XM_005262821.4:c.1307+180_1307+181del	XP_005262878.1:n.1307+180_1307+181del
XM_005262822.4:c.1307+180_1307+181del	XP_005262879.1:n.1307+180_1307+181del
XM_005262823.4:c.1037+180_1037+181del	XP_005262880.1:n.1037+180_1037+181del
XM_006714137.3:c.1259+180_1259+181del	XP_006714200.1:n.1259+180_1259+181del
XR_001741172.2:n.1778+180_1778+181del
NM_000128.4:c.1304+180_1304+181del MANE Select	NP_000119.1:n.1304+180_1304+181del