Canonical Allele Identifier: CA2672902492

Gene: F11

Linked Data

• gnomAD v4: 4-186284236-TAAC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284238_186284240del , CM000666.2:g.186284238_186284240del	GRCh38
NC_000004.11:g.187205392_187205394del , CM000666.1:g.187205392_187205394del	GRCh37
NC_000004.10:g.187442386_187442388del	NCBI36
NG_008051.1:g.23275_23277del , LRG_583:g.23275_23277del

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1282_1284del MANE Select	ENSP00000384957.2:p.Thr428del
ENST00000264692.8:c.1120_1122del	ENSP00000264692.5:p.Thr374del
ENST00000403665.6:c.1282_1284del	ENSP00000384957.2:p.Thr428del
NM_000128.3:c.1282_1284del , LRG_583t1:c.1282_1284del	NP_000119.1:p.Thr428del
XM_005262821.2:c.1285_1287del	XP_005262878.1:p.Thr429del
XM_005262822.2:c.1285_1287del	XP_005262879.1:p.Thr429del
XM_005262823.2:c.1015_1017del	XP_005262880.1:p.Thr339del
XM_005262824.1:c.1285_1287del	XP_005262881.1:p.Thr429del
XM_006714137.1:c.1237_1239del	XP_006714200.1:p.Thr413del
XR_938706.1:n.1690_1692del
XR_938707.1:n.1690_1692del
XM_005262821.4:c.1285_1287del	XP_005262878.1:p.Thr429del
XM_005262822.4:c.1285_1287del	XP_005262879.1:p.Thr429del
XM_005262823.4:c.1015_1017del	XP_005262880.1:p.Thr339del
XM_006714137.3:c.1237_1239del	XP_006714200.1:p.Thr413del
XR_001741172.2:n.1756_1758del
NM_000128.4:c.1282_1284del MANE Select	NP_000119.1:p.Thr428del