Canonical Allele Identifier: CA1519939955
Gene: F11 HGNC NCBI
F11-AS1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186288828_186288830delinsCTT , CM000666.2:g.186288828_186288830delinsCTT GRCh38
NC_000004.11:g.187209982_187209984delinsCTT , CM000666.1:g.187209982_187209984delinsCTT GRCh37
NC_000004.10:g.187446976_187446978delinsCTT NCBI36
NG_008051.1:g.27865_27867delinsCTT , LRG_583:g.27865_27867delinsCTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000403665.7:c.*214_*216delinsCTT (F11) MANE Select ENSP00000384957.2:n.*214_*216delinsCTT
NM_000128.3:c.*214_*216delinsCTT , LRG_583t1:c.*214_*216delinsCTT (F11) NP_000119.1:n.*214_*216delinsCTT
NR_033900.1:n.664_666delinsAAG (F11-AS1)
XM_005262821.2:c.*214_*216delinsCTT (F11) XP_005262878.1:n.*214_*216delinsCTT
XM_005262822.2:c.*214_*216delinsCTT (F11) XP_005262879.1:n.*214_*216delinsCTT
XM_005262823.2:c.*214_*216delinsCTT (F11) XP_005262880.1:n.*214_*216delinsCTT
XM_006714137.1:c.*214_*216delinsCTT (F11) XP_006714200.1:n.*214_*216delinsCTT
XM_005262821.4:c.*214_*216delinsCTT (F11) XP_005262878.1:n.*214_*216delinsCTT
XM_005262822.4:c.*214_*216delinsCTT (F11) XP_005262879.1:n.*214_*216delinsCTT
XM_005262823.4:c.*214_*216delinsCTT (F11) XP_005262880.1:n.*214_*216delinsCTT
XM_006714137.3:c.*214_*216delinsCTT (F11) XP_006714200.1:n.*214_*216delinsCTT
NM_000128.4:c.*214_*216delinsCTT (F11) MANE Select NP_000119.1:n.*214_*216delinsCTT
Search 100 bp 5'
Search 100 bp 3'