Canonical Allele Identifier: CA2764876755

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284159_186284160del , CM000666.2:g.186284159_186284160del	GRCh38
NC_000004.11:g.187205313_187205314del , CM000666.1:g.187205313_187205314del	GRCh37
NC_000004.10:g.187442307_187442308del	NCBI36
NG_008051.1:g.23196_23197del , LRG_583:g.23196_23197del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1203_1204del MANE Select	ENSP00000384957.2:p.Trp401Ter
ENST00000264692.8:c.1041_1042del	ENSP00000264692.5:p.Trp347Ter
ENST00000403665.6:c.1203_1204del	ENSP00000384957.2:p.Trp401Ter
NM_000128.3:c.1203_1204del , LRG_583t1:c.1203_1204del	NP_000119.1:p.Trp401Ter
XM_005262821.2:c.1206_1207del	XP_005262878.1:p.Trp402Ter
XM_005262822.2:c.1206_1207del	XP_005262879.1:p.Trp402Ter
XM_005262823.2:c.936_937del	XP_005262880.1:p.Trp312Ter
XM_005262824.1:c.1206_1207del	XP_005262881.1:p.Trp402Ter
XM_006714137.1:c.1158_1159del	XP_006714200.1:p.Trp386Ter
XR_938706.1:n.1611_1612del
XR_938707.1:n.1611_1612del
XM_005262821.4:c.1206_1207del	XP_005262878.1:p.Trp402Ter
XM_005262822.4:c.1206_1207del	XP_005262879.1:p.Trp402Ter
XM_005262823.4:c.936_937del	XP_005262880.1:p.Trp312Ter
XM_006714137.3:c.1158_1159del	XP_006714200.1:p.Trp386Ter
XM_017007884.2:c.*2175_*2176del	XP_016863373.1:n.*2175_*2176del
XM_017007885.2:c.*71_*72del	XP_016863374.1:n.*71_*72del
XR_001741172.2:n.1677_1678del
NM_000128.4:c.1203_1204del MANE Select	NP_000119.1:p.Trp401Ter