Canonical Allele Identifier: CA1519938010

Gene: F11

Linked Data

• dbSNP Id: rs1741057723

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284679_186284681del , CM000666.2:g.186284679_186284681del	GRCh38
NC_000004.11:g.187205833_187205835del , CM000666.1:g.187205833_187205835del	GRCh37
NC_000004.10:g.187442827_187442829del	NCBI36
NG_008051.1:g.23716_23718del , LRG_583:g.23716_23718del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1304+419_1304+421del MANE Select	ENSP00000384957.2:n.1304+419_1304+421del
ENST00000264692.8:c.1142+419_1142+421del	ENSP00000264692.5:n.1142+419_1142+421del
ENST00000403665.6:c.1304+419_1304+421del	ENSP00000384957.2:n.1304+419_1304+421del
NM_000128.3:c.1304+419_1304+421del , LRG_583t1:c.1304+419_1304+421del	NP_000119.1:n.1304+419_1304+421del
XM_005262821.2:c.1307+419_1307+421del	XP_005262878.1:n.1307+419_1307+421del
XM_005262822.2:c.1307+419_1307+421del	XP_005262879.1:n.1307+419_1307+421del
XM_005262823.2:c.1037+419_1037+421del	XP_005262880.1:n.1037+419_1037+421del
XM_005262824.1:c.1307+419_1307+421del	XP_005262881.1:n.1307+419_1307+421del
XM_006714137.1:c.1259+419_1259+421del	XP_006714200.1:n.1259+419_1259+421del
XR_938706.1:n.1712+419_1712+421del
XR_938707.1:n.1712+419_1712+421del
XM_005262821.4:c.1307+419_1307+421del	XP_005262878.1:n.1307+419_1307+421del
XM_005262822.4:c.1307+419_1307+421del	XP_005262879.1:n.1307+419_1307+421del
XM_005262823.4:c.1037+419_1037+421del	XP_005262880.1:n.1037+419_1037+421del
XM_006714137.3:c.1259+419_1259+421del	XP_006714200.1:n.1259+419_1259+421del
XR_001741172.2:n.1778+419_1778+421del
NM_000128.4:c.1304+419_1304+421del MANE Select	NP_000119.1:n.1304+419_1304+421del